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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by year, source, volume, issue, page.
Page 1: 1 2 3 4 5 6 7 8 9
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1 | 0 | 1 | 1 1967 NEW PHYTOLOGIST 66(1):138-& CORNER EJH VANSTEENIS,CGG - PACIFIC PLANT AREAS 2 | 0 | 0 |
| 2 | 0 | 0 | 2 1976 GASTROENTEROLOGY 70(5):875-875 SILVA LCD; SETTE H; ANTONACIO F; STRASSMAN P; LOPES JD COMMERCIAL GAMMAGLOBULIN (CGG) AS A POSSIBLE VEHICLE OF TRANSMISSION OF HB-S AG IN FAMILIAL CLUSTERING | 0 | 0 |
| 3 | 0 | 0 | 3 1979 PSYCHOPHYSIOLOGY 16(2):194-195 HOLZL R NON-INVASIVE MEASUREMENT OF GASTRIC-MOTILITY BY CONJOINT GASTROGRAPHY (CGG) - METHOD AND PSYCHO-PHYSIOLOGICAL APPLICATIONS | 0 | 0 |
| 4 | 0 | 1 | 4 1980 AMERICAN JOURNAL OF HUMAN GENETICS 32(6):A73-A73 JACKY PB EXPRESSION IN FIBROBLAST-CULTURE OF THE FRAGILE X-CHROMOSOME ASSOCIATED WITH FAMILIAL SEX-LINKED MENTAL-RETARDATION - FACTORS INFLUENCING A RELIABLE DETERMINATION OF THE FREQUENCY OF EXPRESSION | 0 | 0 |
| 5 | 0 | 0 | 5 1980 AMERICAN JOURNAL OF HUMAN GENETICS 32(6):A114-A114 KAISERMCCAW B; HECHT F THE FRAGILE-X - NO DYSMORPHIC SYNDROME, BUT A MARKER | 2 | 2 |
| 6 | 0 | 6 | 6 1980 AMERICAN JOURNAL OF MEDICAL GENETICS 7(4):503-505 KAISERMCCAW B; HECHT F; CADIEN JD; MOORE BC FRAGILE X-LINKED MENTAL-RETARDATION | 14 | 22 |
| 7 | 0 | 0 | 7 1980 ARIZONA MEDICINE 37(11):764-766 HECHT F; KAISERMCCAW B; MOORE BC; CADIEN J; GLOVER TW THE FRAGILE X-CHROMOSOME MENTAL-RETARDATION AND LARGE TESTES | 2 | 2 |
| 8 | 0 | 24 | 8 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(5):752-761 MARENI C; MIGEON BR FRAGILE-X SYNDROME - SEARCH FOR PHENOTYPIC MANIFESTATIONS AT LOCI FOR HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE AND GLUCOSE-6-PHOSPHATE-DEHYDROGENASE | 7 | 10 |
| 9 | 0 | 0 | 9 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A99-A99 BRYANT EM; HOEHN H; MARTIN GM EXPRESSION OF THE FRAGILE X IN EUPLOID SOMATIC-CELL HYBRIDS | 3 | 3 |
| 10 | 0 | 0 | 10 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A100-A100 CARPENTER NJ; LEICHTMAN LG; LOGAN A; SAY B FRAGILE X-LINKED MENTAL-RETARDATION | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 11 | 0 | 0 | 11 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A107-A107 HOWARDPEEBLES PN; FINLEY WH TESTICULAR AND CYTOGENETIC SCREENING OF RETARDED MALES FROM THE SOUTH FOR THE FRAGILE X-LINKED MENTAL-RETARDATION SYNDROME | 1 | 1 |
| 12 | 0 | 0 | 12 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A122-A122 SHAPIRO LR; KUHR MD; WILMOT PL; LILIENTHAL ER; HIGGS LC MULTIPLE SIBLING MENTAL-RETARDATION AND THE IMPACT OF THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 13 | 0 | 0 | 13 1981 ANGLO-WELSH REVIEW (68):6-9 WESTLEY M 'FRAGILE-X' | 0 | 0 |
| 14 | 0 | 0 | 14 1981 BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE 165(9):1197-1206 LEJEUNE J MONOCARBONS METABOLISM AND FRAGILE-X SYNDROME | 22 | 30 |
| 15 | 0 | 0 | 15 1981 CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES 8(2):191-191 SERGOVICH F; POZSONYI J; HINTON G RECENT ADVANCES IN MENTAL-RETARDATION THE FRAGILE X-CHROMOSOME | 1 | 0 |
| 16 | 0 | 19 | 16 1981 CLINICAL GENETICS 19(2):101-110 GUSTAVSON KH; HOLMGREN G; BLOMQUIST HK; MIKKELSEN M; NORDENSON I; et al. FAMILIAL X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOMES IN 2 SWEDISH FAMILIES | 28 | 42 |
| 17 | 0 | 2 | 17 1981 CLINICAL GENETICS 19(2):140-141 SOUDEK D; GORZNY N NO FRAGILE X-CHROMOSOME IN NORMAL MEN | 1 | 3 |
| 18 | 0 | 0 | 18 1981 CLINICAL GENETICS 19(6):493-493 NIELSEN KB; TOMMERUP N; POULSEN H; MIKKELSEN M DANISH FAMILIES WITH X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOME | 1 | 1 |
| 19 | 2 | 4 | 19 1981 CLINICAL GENETICS 20(1):78-78 HOWARDPEEBLES PN FRAGILE-X CHROMOSOME IN NORMAL MALES | 4 | 7 |
| 20 | 0 | 0 | 20 1981 CLINICAL RESEARCH 29(1):A134-A134 HERBST DS; GERRARD JW; DUNN HG; DILL FJ; KALOUSEK DK; et al. NONSPECIFIC X-LINKED MENTAL-RETARDATION, MACRO-ORCHIDISM AND THE FRAGILE X-CHROMOSOME MARKER | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 21 | 1 | 17 | 21 1981 HUMAN GENETICS 59(2):166-169 MATTEI MG; MATTEI JF; VIDAL I; GIRAUD F EXPRESSION IN LYMPHOCYTE AND FIBROBLAST-CULTURE OF THE FRAGILE X-CHROMOSOME - A NEW TECHNICAL APPROACH | 44 | 83 |
| 22 | 0 | 3 | 22 1981 HUMAN GENETICS 59(2):186-186 FONATSCH C A SIMPLE METHOD TO DEMONSTRATE THE FRAGILE X-CHROMOSOME IN FIBROBLASTS | 21 | 38 |
| 23 | 2 | 40 | 23 1981 HUMAN GENETICS 59(4):281-289 MATTEI JF; MATTEI MG; AUMERAS C; AUGER M; GIRAUD F X-LINKED MENTAL-RETARDATION WITH THE FRAGILE-X - A STUDY OF 15 FAMILIES | 48 | 72 |
| 24 | 0 | 23 | 24 1981 JOURNAL OF MEDICAL GENETICS 18(5):366-373 PROOPS R; WEBB T THE FRAGILE X-CHROMOSOME IN THE MARTIN-BELL-RENPENNING SYNDROME AND IN MALES WITH OTHER FORMS OF FAMILIAL MENTAL-RETARDATION | 20 | 32 |
| 25 | 1 | 7 | 25 1981 JOURNAL OF MENTAL DEFICIENCY RESEARCH 25(DEC):253-& RICHARDS BW; SYLVESTER PE; BROOKER C FRAGILE X-LINKED MENTAL-RETARDATION - THE MARTIN-BELL SYNDROME | 37 | 56 |
| 26 | 0 | 9 | 26 1981 LANCET 1(8219):556-557 SOUDEK D; MCGREGOR T SOURCES OF ERROR IN FRAGILE-X DETERMINATION | 6 | 9 |
| 27 | 0 | 9 | 27 1981 LANCET 1(8219):557-557 EBERLE G; ZANKL H; ZANKL M SOURCES OF ERROR IN FRAGILE-X DETERMINATION | 4 | 8 |
| 28 | 0 | 0 | 28 1981 LANCET 1(8223):780-780 DAKER MG; CHIDIAC P; FEAR CN; BERRY AC FRAGILE X IN A NORMAL-MALE - A CAUTIONARY TALE | 52 | 84 |
| 29 | 0 | 4 | 29 1981 LANCET 2(8254):1055-1055 BROWN WT; MEZZACAPPA PM; JENKINS EC SCREENING FOR FRAGILE X SYNDROME BY TESTICULAR SIZE MEASUREMENT | 16 | 23 |
| 30 | 1 | 1 | 30 1981 LANCET 2(8257):1231-1232 WEBB GC; ROGERS JG; PITT DB; HALLIDAY J; THEOBALD T TRANSMISSION OF FRAGILE (X) (Q27) SITE FROM A MALE | 40 | 66 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 31 | 1 | 4 | 31 1981 LANCET 2(8258):1292-1292 JENKINS EC; BROWN WT; DUNCAN CJ; BROOKS J; BENYISHAY M; et al. FEASIBILITY OF FRAGILE X-CHROMOSOME PRENATAL-DIAGNOSIS DEMONSTRATED | 56 | 77 |
| 32 | 1 | 7 | 32 1981 LYON MEDICAL 246(20):428-429 [Anon] MENTAL-RETARDATION DUE TO A FRAGILE X-CHROMOSOME | 0 | 0 |
| 33 | 1 | 7 | 33 1981 NEW ENGLAND JOURNAL OF MEDICINE 305(22):1348-1348 NIELSEN KB; TOMMERUP N; DYGGVE H; SCHOU C MACROORCHIDISM, MENTAL-RETARDATION, AND THE FRAGILE-X | 8 | 12 |
| 34 | 0 | 0 | 34 1981 PEDIATRIC RESEARCH 15(4):560-560 CARPENTER NJ; LEICHTMAN LG; SAY B STUDIES ON THE FRAGILE X-SYNDROME IN SUBJECTS WITH MENTAL-RETARDATION OF UNKNOWN ETIOLOGY | 0 | 0 |
| 35 | 0 | 0 | 35 1981 PEDIATRIC RESEARCH 15(4):569-569 SHAPIRO LR; KUHR MD; WILMOT PL MULTIPLE SIBLING MENTAL-RETARDATION AND THE IMPACT OF THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 36 | 0 | 0 | 36 1981 PEDIATRIC RESEARCH 15(4):645-645 PUESCHEL SM; HAYS R; MENDOZA T A FAMILIAL X-LINKED MENTAL-RETARDATION SYNDROME ASSOCIATED WITH MULTIPLE CONGENITAL-ANOMALIES, MEGALOGENITALIA AND A FRAGILE X-CHROMOSOME | 1 | 1 |
| 37 | 1 | 15 | 37 1981 PEDIATRICS 68(4):594-595 GERALD PS X-LINKED MENTAL-RETARDATION AND THE FRAGILE-X SYNDROME | 5 | 11 |
| 38 | 1 | 30 | 38 1982 AMERICAN JOURNAL OF DISEASES OF CHILDREN 136(5):389-391 TOWNES PL FRAGILE-X SYNDROME - A JIGSAW PUZZLE WITH PICTURE EMERGING | 6 | 8 |
| 39 | 2 | 35 | 39 1982 AMERICAN JOURNAL OF DISEASES OF CHILDREN 136(5):392-398 CARPENTER NJ; LEICHTMAN LG; SAY B FRAGILE X-LINKED MENTAL-RETARDATION - A SURVEY OF 65 PATIENTS WITH MENTAL-RETARDATION OF UNKNOWN ORIGIN | 49 | 65 |
| 40 | 0 | 18 | 40 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(2):286-293 UCHIDA IA; JOYCE EM ACTIVITY OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS | 0 | 66 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 41 | 0 | 0 | 41 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A82-A82 BROWN T; JENKINS E; FRIEDMAN E; BROOKS J; DUNCAN C; et al. A CONTROLLED TRIAL OF FOLIC-ACID THERAPY IN FRAGILE-X INDIVIDUALS | 3 | 3 |
| 42 | 0 | 0 | 42 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A93-A93 HAVKIN S; CHAKI R; GOLDMAN B FRAGILE X-CHROMOSOME IN 2 FAMILIES WITH X-LINKED MENTAL-RETARDATION | 1 | 1 |
| 43 | 0 | 0 | 43 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A103-A103 NOLIN S; BROWN T; JENKINS E FRAGILE-X SYNDROME - DILEMMAS FOR GENETIC-COUNSELING | 1 | 1 |
| 44 | 0 | 0 | 44 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A110-A110 SHAPIRO LR; HASEN J; GORDON G; SOUTHREN AL; WILMOT PL; et al. TESTICULAR INSUFFICIENCY AND DISORDERED THYROID METABOLISM IN THE FRAGILE X-CHROMOSOME SYNDROME | 5 | 7 |
| 45 | 0 | 0 | 45 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A121-A121 CHUDLEY AE; KNOLL J; GERRARD JW; SHEPEL L; MCGAHEY E; et al. FRAGILE X-LINKED MENTAL-RETARDATION - EFFECT OF AGE AND INTELLIGENCE ON EXPRESSION OF FRAGILE-X | 1 | 1 |
| 46 | 0 | 3 | 46 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A129-A129 HOWARDPEEBLES PN FRAGILE X-CHROMOSOME - THE ROLE OF METHIONINE AND OTHER INVITRO MANIPULATIONS | 4 | 5 |
| 47 | 0 | 3 | 47 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A130-A130 JENKINS E; BROWN T; DUNCAN C; BROOKS J FRAGILE X-CHROMOSOME PRENATAL-DIAGNOSIS | 3 | 4 |
| 48 | 0 | 0 | 48 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A131-A131 KNOLL J; CHUDLEY AE; GERRARD JW EFFICACY OF FUDR IN ENHANCING EXPRESSION OF FRA(X) IN AFFECTED MALES AND CARRIER FEMALES WITH FRAGILE X-LINKED MENTAL-RETARDATION | 1 | 1 |
| 49 | 0 | 1 | 49 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A149-A149 WANG JC; BOSS GR; MAGNER MT; ERBE RW FOLATE PATHWAYS IN CELLS FROM FRAGILE-X SYNDROME PATIENTS AND CARRIERS | 2 | 3 |
| 50 | 0 | 0 | 50 1982 AMERICAN JOURNAL OF MEDICAL GENETICS 11(4):489-495 HECHT F; JACKY PB; SUTHERLAND GR THE FRAGILE X-CHROMOSOME - CURRENT METHODS | 16 | 35 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 51 | 1 | 20 | 51 1982 AMERICAN JOURNAL OF MEDICAL GENETICS 13(2):139-148 BROOKWELL R; DANIEL A; TURNER G; FISHBURN J THE FRAGILE X(Q27) FORM OF X-LINKED MENTAL-RETARDATION - FUDR AS AN INDUCING AGENT FOR FRA(X)(Q27) EXPRESSION IN LYMPHOCYTES, FIBROBLASTS, AND AMNIOCYTES | 24 | 49 |
| 52 | 0 | 2 | 52 1982 ANNALES DE GENETIQUE 25(3):149-151 LEJEUNE J; LEGRAND N; LAFOURCADE J; RETHORE MO; RAOUL O; et al. THE FRAGILE X - EFFECT OF TRIMETHOPRIME TREATMENT | 15 | 24 |
| 53 | 16 | 81 | 53 1982 ARCHIVES FRANCAISES DE PEDIATRIE 39(8):633-639 MATTEI JF FRAGILE X-LINKED MENTAL-RETARDATION | 3 | 3 |
| 54 | 0 | 0 | 54 1982 BEHAVIOR GENETICS 12(6):599-599 THEOBALD TM; HAY DA BEHAVIORAL-CORRELATES OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 55 | 0 | 32 | 55 1982 CANADIAN MEDICAL ASSOCIATION JOURNAL 127(2):123-126 LARBRISSEAU A; JEAN P; MESSIER B; RICHER CL FRAGILE X-CHROMOSOME AND X-LINKED MENTAL-RETARDATION | 6 | 9 |
| 56 | 0 | 0 | 56 1982 CLINICAL RESEARCH 30(2):A291-A291 BROWN WT; JENKINS EC; FRIEDMAN E; WISNIEWSKI K; FRENCH JH THE FRAGILE X-SYNDROME - A GENETIC CAUSE OF AUTISM | 0 | 0 |
| 57 | 0 | 0 | 57 1982 CLINICAL RESEARCH 30(2):A292-A292 JENKINS EC; BROWN WT; DUNCAN CJ; BROOKS J DEMONSTRATION OF THE FRAGILE X-CHROMOSOME IN AMNIOTIC-FLUID CELLS | 1 | 2 |
| 58 | 0 | 0 | 58 1982 CLINICAL RESEARCH 30(5):A890-A890 KRUMDIECK CL; HOWARDPEEBLES PN THE ORIGIN OF THE FRAGILE X IN HUMAN-CHROMOSOMES - AN HYPOTHESIS | 0 | 0 |
| 59 | 0 | 0 | 59 1982 CLINICAL RESEARCH 30(5):A891-A891 MIXON C; DEV V EFFECT OF FUDR AND METHIONINE ON THE EXPRESSION OF FRAGILE X IN A LYMPHOBLASTOID CELL-LINE | 1 | 1 |
| 60 | 0 | 0 | 60 1982 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 24(2):252-253 SERGOVICH F; POZSONYI J; HINTON GG RECENT ADVANCES IN MENTAL-RETARDATION - THE FRAGILE X-CHROMOSOME | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 61 | 1 | 5 | 61 1982 HOSPITAL PRACTICE 17(7):17-& BROWN WT; JENKINS EC FRAGILE X - ITS DETECTABILITY | 1 | 1 |
| 62 | 0 | 5 | 62 1982 HUMAN GENETICS 60(1):80-81 ZANKL H; EBERLE G METHODS OF INCREASING THE VISIBILITY OF FRAGILE-X CHROMOSOMES | 5 | 8 |
| 63 | 4 | 23 | 63 1982 HUMAN GENETICS 61(2):113-117 NIELSEN KB; TOMMERUP N; DYGGVE HV; SCHOU C MACRO-ORCHIDISM AND FRAGILE-X IN MENTALLY-RETARDED MALES - CLINICAL, CYTOGENETIC, AND SOME HORMONAL INVESTIGATIONS IN MENTALLY-RETARDED MALES, INCLUDING 2 WITH THE FRAGILE SITE AT XQ28, FRA(X)(Q28) | 12 | 22 |
| 64 | 2 | 6 | 64 1982 HUMAN GENETICS 61(2):160-162 STEINBACH P; BARBI G; BOLLER T ON THE FREQUENCY OF TELOMERIC CHROMOSOMAL CHANGES INDUCED BY CULTURE CONDITIONS SUITABLE FOR FRAGILE-X EXPRESSION | 17 | 31 |
| 65 | 2 | 7 | 65 1982 HUMAN GENETICS 61(2):163-164 EBERLE G; ZANKL H; ZANKL M CO-CULTIVATION STUDIES WITH CELLS OF PATIENTS BEARING FRAGILE-X CHROMOSOMES | 7 | 11 |
| 66 | 2 | 5 | 66 1982 HUMAN GENETICS 61(3):254-255 EBERLE G; ZANKL M; ZANKL H THE EXPRESSION OF FRAGILE X-CHROMOSOMES IN MEMBERS OF THE SAME FAMILY AT DIFFERENT TIMES OF EXAMINATION | 12 | 14 |
| 67 | 2 | 3 | 67 1982 HUMAN GENETICS 61(3):262-263 FRYNS JP; VANDENBERGHE H TRANSMISSION OF FRAGILE (X)(Q27) FROM NORMAL MALE(S) | 26 | 36 |
| 68 | 1 | 12 | 68 1982 HUMAN GENETICS 62(3):282-284 HOWELL RT; MCDERMOTT A REPLICATION STATUS OF THE FRAGILE X-CHROMOSOME, FRA(X) (Q27), IN 3 HETEROZYGOUS FEMALES | 22 | 31 |
| 69 | 5 | 13 | 69 1982 HUMAN GENETICS 62(3):285-286 SCHMIDT A; PASSARGE E; SEEMANOVA E; MACEK M PRENATAL DETECTION OF A FETUS HEMIZYGOUS FOR THE FRAGILE X-CHROMOSOME | 12 | 18 |
| 70 | 8 | 46 | 70 1982 JOHNS HOPKINS MEDICAL JOURNAL 151(5):231-237 PYERITZ RE; STAMBERG J; THOMAS GH; BELL BB; ZAHKA KG; et al. THE MARKER XQ28 SYNDROME (FRAGILE-X SYNDROME) IN A RETARDED MAN WITH MITRAL-VALVE PROLAPSE | 8 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 71 | 0 | 29 | 71 1982 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 12(3):295-301 MERYASH DL; SZYMANSKI LS; GERALD PS INFANTILE-AUTISM ASSOCIATED WITH THE FRAGILE-X SYNDROME | 44 | 71 |
| 72 | 5 | 23 | 72 1982 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 12(3):303-308 BROWN WT; JENKINS EC; FRIEDMAN E; BROOKS J; WISNIEWSKI K; et al. AUTISM IS ASSOCIATED WITH THE FRAGILE-X SYNDROME | 82 | 124 |
| 73 | 0 | 15 | 73 1982 JOURNAL OF MEDICAL GENETICS 19(1):44-48 WEBB GC; HALLIDAY JL; PITT DB; JUDGE CG; LEVERSHA M FRAGILE (X)(Q27) SITES IN A PEDIGREE WITH FEMALE CARRIERS SHOWING MILD TO SEVERE MENTAL-RETARDATION | 19 | 36 |
| 74 | 0 | 0 | 74 1982 JOURNAL OF MEDICAL GENETICS 19(1):64-64 DAKER MG; CHIDIAC P; FEAR CN; BERRY AC FRAGILE X-CHROMOSOME IN BROTHERS WITH NORMAL INTELLIGENCE, OR THE MAN WHO MIGHT HAVE BEEN A GENIUS | 0 | 2 |
| 75 | 0 | 0 | 75 1982 JOURNAL OF MEDICAL GENETICS 19(5):371-371 WILLATT LR; DAVIS J FRAGILE-X MENTAL-RETARDATION IN TWINS - A CASE-HISTORY | 0 | 0 |
| 76 | 1 | 3 | 76 1982 LANCET 1(8263):99-100 SHAPIRO LR; WILMOT PL; BRENHOLZ P; LEFF A; MARTINO M; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X CHROMOSOME | 38 | 59 |
| 77 | 2 | 8 | 77 1982 LANCET 1(8263):100-100 BROWN WT; FRIEDMAN E; JENKINS EC; BROOKS J; WISNIEWSKI K; et al. ASSOCIATION OF FRAGILE-X SYNDROME WITH AUTISM | 50 | 77 |
| 78 | 2 | 8 | 78 1982 LANCET 1(8263):100-100 SUTHERLAND GR; JACKY PB PRENATAL-DIAGNOSIS OF FRAGILE-X CHROMOSOME | 6 | 13 |
| 79 | 0 | 4 | 79 1982 LANCET 1(8263):101-101 GARDNER AP; HOWELL RT; MCDERMOTT A FRAGILE-X CHROMOSOME - CONSISTENT DEMONSTRATION OF FRAGILE SITE IN FIBROBLAST-CULTURES | 10 | 14 |
| 80 | 4 | 9 | 80 1982 LANCET 1(8266):273-274 LEJEUNE J IS THE FRAGILE-X SYNDROME AMENABLE TO TREATMENT | 47 | 62 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 81 | 0 | 0 | 81 1982 LANCET 2(8307):1104-1104 KINNELL HG FRAGILE-X DISORDER ASSOCIATED WITH ANTISOCIAL PERSONALITY | 3 | 5 |
| 82 | 0 | 0 | 82 1982 NEUROLOGY 32(4):A190-A190 ROSENBERGER PB; WILSONCIAMBRONE S; MILUNSKY A SPEECH FLUENCY DISORDER IN THE FRAGILE-X SYNDROME | 2 | 2 |
| 83 | 1 | 6 | 83 1982 NEW ENGLAND JOURNAL OF MEDICINE 306(25):1551-1552 POPOVICH B; VEKEMANS M; ROSENBLATT D; MONROE P FRAGILE-X | 17 | 21 |
| 84 | 1 | 7 | 84 1982 PEDIATRICS 69(5):668-669 RHOADS FA X-LINKED MENTAL-RETARDATION AND FRAGILE-X OR MARKER-X SYNDROME | 11 | 12 |
| 85 | 0 | 0 | 85 1982 PEDIATRICS 69(5):669-669 GERALD PS X-LINKED MENTAL-RETARDATION AND FRAGILE-X OR MARKER-X SYNDROME - REPLY | 1 | 1 |
| 86 | 0 | 0 | 86 1982 PEDIATRICS 69(5):670-670 HARPEY JP TREATMENT OF FRAGILE-X | 19 | 24 |
| 87 | 5 | 37 | 87 1982 WESTERN JOURNAL OF MEDICINE 137(4):278-281 MOORE BC; GLOVER TW; KAISERMCCAW B; HECHT F FRAGILE X-LINKED MENTAL-RETARDATION AND MACRO-ORCHIDISM | 1 | 3 |
| 88 | 0 | 21 | 88 1982 WIENER KLINISCHE WOCHENSCHRIFT 94(8):217-219 FONATSCH C; FLATZ SD FRAGILE X-CHROMOSOME AND X-LINKED MENTAL-RETARDATION | 1 | 1 |
| 89 | 2 | 13 | 89 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(5):861-868 UCHIDA IA; FREEMAN VCP; JAMRO H; PARTINGTON MW; SOLTAN HC ADDITIONAL EVIDENCE FOR FRAGILE-X ACTIVITY IN HETEROZYGOUS CARRIERS | 25 | 33 |
| 90 | 5 | 26 | 90 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(5):869-878 POPOVICH BW; ROSENBLATT DS; COOPER BA; VEKEMANS M INTRACELLULAR FOLATE DISTRIBUTION IN CULTURED FIBROBLASTS FROM PATIENTS WITH THE FRAGILE-X SYNDROME | 8 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 91 | 0 | 0 | 91 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A81-A81 BROWN T; JENKINS E; SHAPIRO LR FRAGILE (X) SYNDROME PRENATAL-DIAGNOSIS REGISTRY | 0 | 0 |
| 92 | 0 | 1 | 92 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A82-A82 CARPENTER NJ; BARBER DH; JONES M; LINDLEY W; CARR C CONTROLLED 6-MONTH STUDY OF ORAL FOLIC-ACID THERAPY IN BOYS WITH FRAGILE X-LINKED MENTAL-RETARDATION | 0 | 9 |
| 93 | 0 | 0 | 93 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A92-A92 HAGERMAN R; MCBOGG P; LEVITUS A; MCGAVRAN L; SMITH A; et al. FOLIC-ACID TREATMENT OF THE FRAGILE-X SYNDROME | 3 | 4 |
| 94 | 0 | 0 | 94 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A117-A117 SHAPIRO LR; SUMMA GM; WILMOT PL; GLOTH E SCREENING AND DETECTION OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 95 | 0 | 1 | 95 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A122-A122 WILSON DP; CARPENTER NJ; BERKOVITZ GD; BROWN TR; MIGEON CJ THYROID-FUNCTION IN FRAGILE X-LINKED MENTAL-RETARDATION | 2 | 2 |
| 96 | 0 | 0 | 96 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A127-A127 BRYANT EM; GLADSTONE P; MARTIN GM EXPRESSION OF THE FRAGILE-X IN MOUSE-X HUMAN SOMATIC-CELL HYBRIDS | 2 | 2 |
| 97 | 0 | 0 | 97 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A131-A131 EREN M; DISTECHE C BEHAVIORAL-PHENOTYPE OF THE FRAGILE X-SYNDROME - RELATIONSHIP BETWEEN FREQUENCY OF MARKER-X, MENTAL-RETARDATION AND VERBAL DISABILITY | 3 | 5 |
| 98 | 0 | 0 | 98 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A135-A135 HOWARDPEEBLES PN FRAGILE X-CHROMOSOME - TECHNICAL ASPECTS FOR MAXIMIZING EXPRESSION | 0 | 0 |
| 99 | 0 | 0 | 99 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A136-A136 JENKINS E; DUNCAN C; BROOKS J; LELE K; SANZ M; et al. LOW-FREQUENCY FRAGILE X-CHROMOSOMES IN CULTURES FROM NORMAL PEOPLE | 0 | 4 |
| 100 | 0 | 0 | 100 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A139-A139 KNOLL JH; CHUDLEY AE; GERRARD JW FREQUENCY AND REPLICATION PATTERN OF FRAGILE (X) (Q28) IN HETEROZYGOTES | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 101 | 0 | 2 | 101 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A144-A144 MIXON C; DEV VG INHIBITION OF FRAGILE-X EXPRESSION BY 5-AZACYTIDINE (AZA) AND BY S-ADENOSYLHOMOCYSTEINE (SAH) | 0 | 0 |
| 102 | 0 | 0 | 102 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A146-A146 OBRIEN MM; PADREMENDOZA T; PUESCHEL SM MATERNAL NONDISJUNCTION OF FRAGILE X-CHROMOSOME RESULTING IN KLINEFELTER SYNDROME | 1 | 2 |
| 103 | 0 | 0 | 103 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A159-A159 WANG JC; BEARDSLEY GP; ERBE RW THYMIDYLATE METABOLISM AND URACIL MISINCORPORATION IN FRAGILE-X SYNDROME CELLS | 0 | 2 |
| 104 | 0 | 0 | 104 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A161-A161 WILLEY A; HATCHER N; HEALY N FRAGILE-X FAMILIES - GENETIC INSTABILITY, OR UNEXPECTED CYTOGENETIC ABERRATIONS | 0 | 0 |
| 105 | 0 | 0 | 105 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A162-A162 WILSON MG; MARCHESE CA; LIN MS; HERBERT WS; PERDELWITZ M PRENATAL-DIAGNOSIS OF FRAGILE-X IN A HETEROZYGOUS FEMALE FETUS AND POSTNATAL FOLLOW-UP | 0 | 0 |
| 106 | 0 | 0 | 106 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A174-A174 HOLDEN J; BECKETT J; MULLIGAN L; PHILLIPS A; SIMPSON N; et al. A SEARCH FOR RESTRICTION FRAGMENT LENGTH POLYMORPHISMS (RFLPS) LINKED TO THE FRAGILE-X FORM OF X-LINKED MENTAL-RETARDATION | 0 | 3 |
| 107 | 2 | 13 | 107 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):1270-1275 MIXON JC; DEV VG FRAGILE-X EXPRESSION IS DECREASED BY 5-AZACYTIDINE AND S-ADENOSYLHOMOCYSTEINE | 5 | 9 |
| 108 | 8 | 32 | 108 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):699-712 CHUDLEY AE; KNOLL J; GERRARD JW; SHEPEL L; MCGAHEY E; et al. FRAGILE (X) X-LINKED MENTAL-RETARDATION .1. RELATIONSHIP BETWEEN AGE AND INTELLIGENCE AND THE FREQUENCY OF EXPRESSION OF FRAGILE (X)(Q28) | 56 | 80 |
| 109 | 4 | 5 | 109 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):795-796 DAKER MG FRAGILE X-CHROMOSOME IN NORMAL MALES | 2 | 4 |
| 110 | 1 | 1 | 110 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):797-797 HECHT F; JACKY PB; SUTHERLAND GR FRAGILE X-CHROMOSOME IN NORMAL MALES - REPLY | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 111 | 2 | 28 | 111 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 15(1):113-119 FILIPPI G; RINALDI A; ARCHIDIACONO N; ROCCHI M; BALAZS I; et al. LINKAGE BETWEEN G6PD AND FRAGILE-X SYNDROME | 19 | 43 |
| 112 | 1 | 14 | 112 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 15(4):631-635 HOWARDPEEBLES PN; FINLEY WH SCREENING OF MENTALLY-RETARDED MALES FOR MACRO-ORCHIDISM AND THE FRAGILE-X CHROMOSOME | 16 | 22 |
| 113 | 0 | 36 | 113 1983 AMERICAN JOURNAL OF MENTAL DEFICIENCY 87(4):372-376 PUESCHEL SM; HAYS RM; MENDOZA T FAMILIAL X-LINKED MENTAL-RETARDATION SYNDROME ASSOCIATED WITH MINOR CONGENITAL-ANOMALIES, MACRO-ORCHIDISM, AND FRAGILE X-CHROMOSOME | 6 | 8 |
| 114 | 2 | 4 | 114 1983 ANNALES DE GENETIQUE 26(3):147-149 CALVAMERCADO MP; MAUNOURY C; RETHORE MO; LEJEUNE J FRAGILE-X AND INHIBITION OF DIHYDROFOLATE-REDUCTASE - COMPARED EFFECTS OF 2 ANTIBIOTICS - TRIMETHOPRIME AND PYRIMETHAMINE | 6 | 13 |
| 115 | 2 | 15 | 115 1983 ANNALES DE GENETIQUE 26(3):171-173 JACKY PB; DILL FJ FRAGILE-X CHROMOSOME AND CHROMOSOME CONDENSATION | 1 | 4 |
| 116 | 9 | 17 | 116 1983 ANNALES DE GENETIQUE 26(4):247-250 TEJADA I; BOUE J; GILGENKRANTZ S PRENATAL-DIAGNOSIS OF FRAGILE X-CHROMOSOME ON AMNIOTIC-FLUID CELLS | 6 | 9 |
| 117 | 1 | 13 | 117 1983 ANNALES DE GENETIQUE 26(4):251-253 FRYNS JP; KLECZKOWSKA A; KUBIEN E; PETIT P; HASPESLAGH M; et al. XY XXY MOSAICISM AND FRAGILE X-SYNDROME | 12 | 17 |
| 118 | 0 | 1 | 118 1983 BIOLOGY OF THE CELL 48(2-3):A92-A92 LENOARD C; SCHOEVAERT D; SELVA J APPLICATION OF THE AUTOMATIC-ANALYSIS OF METAPHASES TO THE DIAGNOSIS OF THE FRAGILE-X IN MAN | 0 | 0 |
| 119 | 2 | 11 | 119 1983 BRITISH JOURNAL OF PSYCHIATRY 143(SEP):256-260 GILLBERG C IDENTICAL TRIPLETS WITH INFANTILE-AUTISM AND THE FRAGILE-X SYNDROME | 20 | 38 |
| 120 | 0 | 0 | 120 1983 CLINICAL GENETICS 23(3):216-216 MCDERMOTT A MORE ON THE FRAGILE-X, WITH PARTICULAR REFERENCE TO FIBROBLAST AND AMNIOTIC-FLUID CULTURE, AND X-INACTIVATION | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 121 | 1 | 1 | 121 1983 CLINICAL GENETICS 23(3):229-229 FONATSCH C FRAGILE X-CHROMOSOME IN FIBROBLASTS - LONGITUDINAL-STUDY ON TECHNICAL VARIATIONS | 3 | 3 |
| 122 | 0 | 0 | 122 1983 CLINICAL GENETICS 23(3):232-232 VANDERHAGEN CB; ORSTAVIK KH; BAKKE J; BERG K MONOZYGOUS MALE TRIPLETS WITH MENTAL-RETARDATION AND A FRAGILE X-CHROMOSOME | 2 | 2 |
| 123 | 0 | 0 | 123 1983 CLINICAL GENETICS 23(3):236-236 PAJARES IL; DELICADO A; GALLEGO A; CASTROVIEJO IP FAMILIAL X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOMES IN 6 SPANISH FAMILIES | 1 | 1 |
| 124 | 0 | 0 | 124 1983 CLINICAL GENETICS 23(3):241-241 NIELSEN KB; TOMMERUP N; MIKKELSEN M CLINICAL AND CYTOGENETIC FINDINGS IN 26 MENTALLY-RETARDED MALES WITH THE FRAGILE-X | 1 | 1 |
| 125 | 0 | 0 | 125 1983 CLINICAL GENETICS 23(3):250-251 TEJADA I; NICOLAS H; CHERUY C; BOUE J STUDY OF A LARGE SIBSHIP WITH MENTALLY-RETARDED MALES AND FEMALES CARRYING FRAGILE-X | 1 | 1 |
| 126 | 0 | 0 | 126 1983 CLINICAL GENETICS 23(3):254-254 VEENEMA H; GERAEDTS JPM THE FRAGILE-X CHROMOSOME SEGREGATING IN A LARGE PEDIGREE | 2 | 2 |
| 127 | 0 | 0 | 127 1983 CLINICAL GENETICS 23(3):255-255 VERSCHRAEGENSPAE MR; VANDENBOSSCHE H; MATTON MT APPROACH TO RELATIVES IN FRAGILE X-LINKED MENTAL-RETARDATION | 0 | 2 |
| 128 | 5 | 14 | 128 1983 CLINICAL GENETICS 23(4):311-317 GARDNER RJM; SMART RD; CORNELL JM; MERCKEL LM; BEIGHTON P THE FRAGILE X-CHROMOSOME IN A LARGE INDIAN KINDRED | 17 | 20 |
| 129 | 8 | 23 | 129 1983 CLINICAL GENETICS 23(6):436-440 SILVERMAN W; LUBIN R; JENKINS EC; BROWN WT THE STRENGTH OF ASSOCIATION BETWEEN FRAGILE(X) CHROMOSOME PRESENCE AND MENTAL-RETARDATION | 8 | 11 |
| 130 | 3 | 11 | 130 1983 CLINICAL GENETICS 24(3):153-155 NIELSEN KB; TOMMERUP N; FRIIS B; HJELT K; HIPPE E FOLIC-ACID METABOLISM IN A PATIENT WITH FRAGILE-X | 0 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 131 | 1 | 4 | 131 1983 CLINICAL GENETICS 24(5):320-323 DEARCE MA TABLES FOR THE CYTOGENETIC STUDY OF FRAGILE X-CHROMOSOMES FOR DIAGNOSTIC PURPOSES | 11 | 17 |
| 132 | 3 | 15 | 132 1983 CLINICAL GENETICS 24(6):393-398 BLOMQUIST HK; GUSTAVSON KH; HOLMGREN G; NORDENSON I; PALSSONSTRAE U FRAGILE X-SYNDROME IN MILDLY MENTALLY-RETARDED CHILDREN IN A NORTHERN SWEDISH COUNTY - A PREVALENCE STUDY | 43 | 68 |
| 133 | 0 | 0 | 133 1983 CLINICAL RESEARCH 31(2):A290-A290 BRANDA RF; ARTHUR DC; KING RA FRAGILE X PATIENTS HAVE NORMAL FOLATE METABOLISM | 2 | 2 |
| 134 | 0 | 1 | 134 1983 CLINICAL RESEARCH 31(2):A290-A290 BROWN T; JENKINS E; FRIEDMAN E; BROOKS J; DUNCAN C; et al. FOLIC-ACID THERAPY OF FRAGILE-X SYNDROME | 0 | 0 |
| 135 | 0 | 1 | 135 1983 CLINICAL RESEARCH 31(5):A897-A897 HOWARDPEEBLES PN NORMAL-MALE TRANSMISSION OF THE FRAGILE-X - THE COUNSELING DILEMMA | 0 | 0 |
| 136 | 1 | 10 | 136 1983 CYTOGENETICS AND CELL GENETICS 35(3):223-225 BRYANT EM; MARTIN GM; HOEHN H FRAGILE-X EXPRESSION STUDIED BY CLONAL ANALYSIS AND SOMATIC-CELL HYBRIDIZATION | 9 | 12 |
| 137 | 8 | 23 | 137 1983 HUMAN GENETICS 64(1):39-41 FONATSCH C; SCHWINGER E FREQUENCY OF FRAGILE-X CHROMOSOMES, FRA(X), IN LYMPHOCYTES IN RELATION TO BLOOD-STORAGE TIME AND CULTURE TECHNIQUES | 6 | 9 |
| 138 | 5 | 17 | 138 1983 HUMAN GENETICS 64(2):148-150 NUSSBAUM RL; AIRHART SD; LEDBETTER DH EXPRESSION OF THE FRAGILE (X)CHROMOSOME IN AN INTERSPECIFIC SOMATIC-CELL HYBRID | 18 | 58 |
| 139 | 6 | 26 | 139 1983 HUMAN GENETICS 64(3):240-245 NIELSEN KB; TOMMERUP N; POULSEN H; JACOBSEN P; BECK B; et al. CARRIER DETECTION AND X-INACTIVATION STUDIES IN THE FRAGILE-X SYNDROME - CYTOGENETIC STUDIES IN 63 OBLIGATE AND POTENTIAL CARRIERS OF THE FRAGILE-X | 23 | 35 |
| 140 | 3 | 9 | 140 1983 HUMAN GENETICS 65(1):88-89 SOUDEK D; EMANUEL M A FRAGILE X SUPPRESSOR IN THE NORMAL HUMAN-BLOOD | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 141 | 24 | 128 | 141 1983 INTERNATIONAL REVIEW OF CYTOLOGY-A SURVEY OF CELL BIOLOGY 81:107-143 SUTHERLAND GR THE FRAGILE X-CHROMOSOME | 39 | 131 |
| 142 | 8 | 28 | 142 1983 IRISH JOURNAL OF MEDICAL SCIENCE 152(12):440-445 DEARCE MA; LAW E; MASTERSON JG NON-SPECIFIC X-LINKED MENTAL-RETARDATION WITH FRAGILE-X CHROMOSOME - SOMATIC FEATURES, CYTOGENETIC DIAGNOSIS AND ELEMENTS FOR GENETIC-COUNSELING | 1 | 3 |
| 143 | 3 | 10 | 143 1983 JOURNAL DE GENETIQUE HUMAINE 31(2):133-139 JALBERT H; BAETEMAN MA; TROCHETROYER C; MATTEI MG; MATTEI JF; et al. MENTAL-RETARDATION WITH FRAGILE-X - NEITHER INACTIVATION NOR DELETION OF THE SEGMENT Q28-]Q TER ENZYMATIC AND MORPHOMETRIC DATA | 0 | 0 |
| 144 | 13 | 68 | 144 1983 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 4(2):122-130 HAGERMAN RJ; MCBOGG P; HAGERMAN PJ THE FRAGILE-X SYNDROME - HISTORY, DIAGNOSIS, AND TREATMENT | 14 | 18 |
| 145 | 7 | 20 | 145 1983 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 4(3):151-158 LEVITAS A; HAGERMAN RJ; BRADEN M; RIMLAND B; MCBOGG P; et al. AUTISM AND THE FRAGILE-X SYNDROME | 49 | 63 |
| 146 | 8 | 31 | 146 1983 JOURNAL OF MEDICAL GENETICS 20(3):169-178 MCDERMOTT A; WALTERS R; HOWELL RT; GARDNER A FRAGILE X-CHROMOSOME - CLINICAL AND CYTOGENETIC STUDIES ON CASES FROM 7 FAMILIES | 14 | 18 |
| 147 | 0 | 11 | 147 1983 JOURNAL OF MEDICAL GENETICS 20(4):280-285 HARRISON CJ; JACK EM; ALLEN TD; HARRIS R THE FRAGILE X - A SCANNING ELECTRON-MICROSCOPE STUDY | 27 | 54 |
| 148 | 4 | 12 | 148 1983 JOURNAL OF MEDICAL GENETICS 20(4):286-289 VANROY BC; DESMEDT MC; RAES RA; DUMON JE; LEROY JG FRAGILE X TRAIT IN A LARGE KINDRED - TRANSMISSION ALSO THROUGH NORMAL MALES | 22 | 32 |
| 149 | 3 | 9 | 149 1983 JOURNAL OF MEDICAL GENETICS 20(4):314-315 HUNTER AGW; MACDONALD J; EVANS JA ABSENCE OF THE FRAGILE-X IN A GROUP OF PATIENTS WITH IDIOPATHIC MENTAL-RETARDATION | 0 | 0 |
| 150 | 5 | 25 | 150 1983 JOURNAL OF MEDICAL GENETICS 20(6):404-407 VEKEMANS M; POPOVICH B; ROSENBLATT D; MONROE P CHROMOSOMAL BREAKAGE IN NORMAL AND FRAGILE-X SUBJECTS USING LOW FOLATE CULTURE CONDITIONS | 12 | 21 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 151 | 0 | 1 | 151 1983 JOURNAL OF MEDICAL GENETICS 20(6):476-476 MORICPETROVIC S; LACA Z A FATHER AND DAUGHTER WITH FRAGILE X-CHROMOSOME | 6 | 7 |
| 152 | 8 | 17 | 152 1983 JOURNAL OF MENTAL DEFICIENCY RESEARCH 27(SEP):211-226 NIELSEN KB DIAGNOSIS OF THE FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) - CLINICAL FINDINGS IN 27 MALES WITH THE FRAGILE SITE AT XQ28 | 18 | 26 |
| 153 | 1 | 9 | 153 1983 LANCET 1(8335):1221-1222 RUDELLI RD; JENKINS EC; WISNIEWSKI K; MORETZ R; BYRNE J; et al. TESTICULAR SIZE IN FETAL FRAGILE X SYNDROME | 14 | 19 |
| 154 | 0 | 4 | 154 1983 LANCET 2(8364):1427-1427 KINNELL HG; BANU SP INSTITUTIONAL PREVALENCE OF FRAGILE X-SYNDROME | 5 | 8 |
| 155 | 0 | 0 | 155 1983 MEDICINA-BUENOS AIRES 43(6):756-756 DELREY G; COCO R INVESTIGATION OF FRAGILE X-CHROMOSOMES IN MEN WITH MENTAL-RETARDATION (RM) OF UNKNOWN CAUSE | 0 | 0 |
| 156 | 8 | 33 | 156 1983 NATURE 306(5944):701-704 CAMERINO G; MATTEI MG; MATTEI JF; JAYE M; MANDEL JL CLOSE LINKAGE OF FRAGILE X MENTAL-RETARDATION SYNDROME TO HEMOPHILIA-B AND TRANSMISSION THROUGH A NORMAL-MALE | 78 | 171 |
| 157 | 2 | 6 | 157 1983 NEW ENGLAND JOURNAL OF MEDICINE 308(5):285-286 HECHT F; GLOVER TW ANTIBIOTICS CONTAINING TRIMETHOPRIM AND THE FRAGILE X-CHROMOSOME | 4 | 6 |
| 158 | 2 | 6 | 158 1983 NEW ENGLAND JOURNAL OF MEDICINE 308(23):1424-1424 HAGERMAN RJ; LEVITAS A DILANTIN AND THE FRAGILE X-SYNDROME | 0 | 2 |
| 159 | 0 | 0 | 159 1983 PATHOLOGY 15(1):105-106 JACKY PB; SUTHERLAND GR FRAGILE-X EXPRESSION IN FIBROBLASTS | 0 | 0 |
| 160 | 0 | 0 | 160 1983 PEDIATRIE 38(3):191-198 JALBERT P FRAGILE X-LINKED MENTAL-RETARDATION - MORE QUESTIONS | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 161 | 7 | 21 | 161 1983 PRENATAL DIAGNOSIS 3(2):131-137 WEBB T; GOSDEN CM; RODECK CH; HAMILL MA; EASON PE PRENATAL-DIAGNOSIS OF X-LINKED MENTAL-RETARDATION WITH FRAGILE (X) USING FETOSCOPY AND FETAL BLOOD-SAMPLING | 16 | 32 |
| 162 | 3 | 8 | 162 1983 PRENATAL DIAGNOSIS 3(4):367-369 NIELSEN LB; NIELSEN KB; TOMMERUP N FRAGILE-X DEMONSTRATED RETROSPECTIVELY IN AMNIOTIC CELLS CULTURED IN LOW FOLATE MEDIUM | 2 | 4 |
| 163 | 6 | 26 | 163 1983 REVISTA MEDICA DE CHILE 111(6):597-600 SANTOS M; MORIZON G THE FRAGILE X SYNDROME - A CHROMOSOMAL DEFECT ASSOCIATED WITH MENTAL-RETARDATION | 0 | 0 |
| 164 | 5 | 52 | 164 1983 SCHWEIZERISCHE MEDIZINISCHE WOCHENSCHRIFT 113(7):238-244 ZOLLINGER A; SCHMID W; VILAN J; SORG B; KNOBLAUCH M X-LINKED MENTAL-RETARDATION WITH FRAGILE X-CHROMOSOME AND MACROORCHIDISM | 3 | 3 |
| 165 | 0 | 0 | 165 1983 TERATOLOGY 28(1):A30-A30 ISHIKIRIYAMA S; NIIKAWA N 2 JAPANESE PATIENTS WITH FRAGILE X SYNDROME | 0 | 2 |
| 166 | 5 | 19 | 166 1984 ACTA PSYCHIATRICA SCANDINAVICA 70(5):510-514 JORGENSEN OS; NIELSEN KB; ISAGER T; MOURIDSEN SE FRAGILE X-CHROMOSOME AMONG CHILD PSYCHIATRIC-PATIENTS WITH DISTURBANCES OF LANGUAGE AND SOCIAL RELATIONSHIPS - A PILOT-STUDY | 12 | 21 |
| 167 | 15 | 52 | 167 1984 ALABAMA JOURNAL OF MEDICAL SCIENCES 21(1):68-72 SCARBROUGH PR; COSPER P; FINLEY SC; SMITH NB FRAGILE-X SYNDROME - AN OVERVIEW | 0 | 3 |
| 168 | 5 | 15 | 168 1984 ALABAMA JOURNAL OF MEDICAL SCIENCES 21(3):284-286 MIXON JC; DEV VG UNDERSTANDING THE FRAGILE X-SYNDROME | 0 | 2 |
| 169 | 0 | 0 | 169 1984 ALABAMA JOURNAL OF MEDICAL SCIENCES 21(3):322-322 MIXON JC INHIBITION OF FRAGILE-X EXPRESSION BY 5-AZACYTIDINE (AZA) AND BY S-ADENOSYLHOMOCYSTEINE (SAH) | 0 | 0 |
| 170 | 0 | 4 | 170 1984 AMERICAN JOURNAL OF HUMAN GENETICS 36(1):227-229 MIEZEJESKI CM; JENKINS EC; HILL AL; WISNIEWSKI K; BROWN WT VERBAL VS NONVERBAL ABILITY, FRAGILE-X SYNDROME, AND HETEROZYGOUS CARRIERS | 8 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 171 | 4 | 19 | 171 1984 AMERICAN JOURNAL OF HUMAN GENETICS 36(3):640-645 KNOLL JH; CHUDLEY AE; GERRARD JW FRAGILE (X) X-LINKED MENTAL-RETARDATION .2. FREQUENCY AND REPLICATION PATTERN OF FRAGILE (X) (Q28) IN HETEROZYGOTES | 20 | 31 |
| 172 | 103 | 406 | 172 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):5-94 OPITZ JM; SUTHERLAND GR CONFERENCE REPORT - INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 52 | 116 |
| 173 | 4 | 16 | 173 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):111-121 HAGERMAN RJ; VANHOUSEN K; SMITH ACM; MCGAVRAN L CONSIDERATION OF CONNECTIVE-TISSUE DYSFUNCTION IN THE FRAGILE-X SYNDROME | 25 | 35 |
| 174 | 1 | 12 | 174 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):123-131 HAGERMAN RJ; SYNHORST DP MITRAL-VALVE PROLAPSE AND AORTIC DILATATION IN THE FRAGILE-X SYNDROME | 9 | 17 |
| 175 | 2 | 16 | 175 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):159-174 MERYASH DL; CRONK CE; SACHS B; GERALD PS AN ANTHROPOMETRIC STUDY OF MALES WITH THE FRAGILE-X SYNDROME | 26 | 43 |
| 176 | 4 | 29 | 176 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):175-194 PARTINGTON MW THE FRAGILE-X SYNDROME .2. PRELIMINARY DATA ON GROWTH AND DEVELOPMENT IN MALES | 52 | 65 |
| 177 | 3 | 25 | 177 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):195-207 SIMPSON NE; NEWMAN BJ; PARTINGTON MW FRAGILE-X SYNDROME .3. DERMATOGLYPHIC STUDIES IN MALES | 10 | 16 |
| 178 | 0 | 4 | 178 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):209-214 RHOADS FA FRAGILE-X SYNDROME IN HAWAII - A SUMMARY OF CLINICAL-EXPERIENCE | 12 | 21 |
| 179 | 10 | 43 | 179 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):215-239 JENKINS EC; BROWN WT; BROOKS J; DUNCAN CJ; RUDELLI RD; et al. EXPERIENCE WITH PRENATAL FRAGILE-X DETECTION | 35 | 44 |
| 180 | 4 | 16 | 180 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):241-252 SOUDEK D; PARTINGTON MW; LAWSON JS THE FRAGILE-X SYNDROME .1. FAMILIAL VARIATION IN THE PROPORTION OF LYMPHOCYTES WITH THE FRAGILE SITE IN MALES | 24 | 29 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 181 | 0 | 2 | 181 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):253-254 DEV VG; MIXON C 5-AZACYTIDINE DECREASES THE FREQUENCY OF FRAGILE-X EXPRESSION IN PERIPHERAL LYMPHOCYTE CULTURE | 4 | 6 |
| 182 | 2 | 11 | 182 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):255-257 DANIEL A; EKBLOM L; PHILLIPS S FRAGILE-X EXPRESSION SUPPRESSED IN EITHER FUDR OR METHOTREXATE TREATED FIBROBLASTS BY PRETREATMENT WITH 5-AZACYTIDINE | 3 | 5 |
| 183 | 3 | 20 | 183 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):259-273 HOLDEN JJA; WANG HS; WHITE BN THE FRAGILE-X SYNDROME .4. PROGRESS TOWARDS THE IDENTIFICATION OF LINKED RESTRICTION FRAGMENT LENGTH VARIANTS (RFLVS) | 4 | 13 |
| 184 | 1 | 2 | 184 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):275-276 HOWARDPEEBLES PN; CARROLL AJ RECOMBINATION BETWEEN THE FRAGILE-X AND G6PD | 1 | 3 |
| 185 | 6 | 13 | 185 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):289-297 BROWN WT; JENKINS EC; FRIEDMAN E; BROOKS J; COHEN IL; et al. FOLIC-ACID THERAPY IN THE FRAGILE-X SYNDROME | 20 | 28 |
| 186 | 3 | 9 | 186 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):299-301 ERBE RW FOLIC-ACID THERAPY IN THE FRAGILE-X SYNDROME | 4 | 8 |
| 187 | 2 | 11 | 187 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):303-310 WANG JCC; ERBE RW FOLATE METABOLISM IN CELLS FROM FRAGILE-X SYNDROME PATIENTS AND CARRIERS | 15 | 22 |
| 188 | 8 | 12 | 188 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(4):853-855 GARDNER RJM FRAGILE-X MALES WITH NORMAL INTELLIGENCE - AND IF SO, WHY | 4 | 7 |
| 189 | 0 | 2 | 189 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(4):857-858 CHUDLEY AE; KNOLL JH; GERRARD JW FRAGILE-X MALES WITH NORMAL INTELLIGENCE - AND IF SO, WHY - REPLY | 0 | 0 |
| 190 | 4 | 13 | 190 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 18(3):483-491 DANIEL A; EKBLOM L; PHILLIPS S CONSTITUTIVE FRAGILE SITES 1P31, 3P14, 6Q26, AND 16Q23 AND THEIR USE AS CONTROLS FOR FALSE-NEGATIVE RESULTS WITH THE FRAGILE(X) | 12 | 50 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 191 | 6 | 36 | 191 1984 AMERICAN JOURNAL OF MEDICINE 77(4):602-611 BRANDA RF; ARTHUR DC; WOODS WG; DANZL TJ; KING RA FOLATE METABOLISM AND CHROMOSOMAL STABILITY IN THE FRAGILE-X SYNDROME | 5 | 14 |
| 192 | 4 | 11 | 192 1984 ANNALES DE GENETIQUE 27(4):230-232 LEJEUNE J; RETHORE MO; DEBLOIS MC; RAVEL A ASSAY OF FOLIC-ACID TREATMENT IN FRAGILE-X SYNDROME | 8 | 13 |
| 193 | 1 | 6 | 193 1984 CHINESE MEDICAL JOURNAL 97(11):861-864 XU BZ; REN S; XIAO GF; ZHOU XT A FRAGILE X SYNDROME FAMILY | 0 | 1 |
| 194 | 0 | 3 | 194 1984 CLINICAL GENETICS 25(2):131-134 FRYNS JP; JACOBS J; KLECZKOWSKA A; VANDENBERGHE H THE PSYCHOLOGICAL PROFILE OF THE FRAGILE X-SYNDROME | 57 | 75 |
| 195 | 1 | 9 | 195 1984 CLINICAL GENETICS 25(2):135-139 GARDINER GB; WENGER SL; STEELE MW INVITRO REVERSAL OF FRAGILE-X EXPRESSION BY EXOGENOUS THYMIDINE | 5 | 7 |
| 196 | 2 | 11 | 196 1984 CLINICAL GENETICS 26(5):445-447 FRYNS JP; KLECZKOWSKA A; WOLFS I; VANDENBERGHE H KLINEFELTER SYNDROME AND 2 FRAGILE X-CHROMOSOMES | 15 | 21 |
| 197 | 21 | 64 | 197 1984 CLINICAL GENETICS 26(6):497-528 FRYNS JP THE FRAGILE X-SYNDROME - A STUDY OF 83 FAMILIES | 45 | 78 |
| 198 | 0 | 0 | 198 1984 CLINICAL RESEARCH 32(5):A884-A884 FRIEDMAN JM; HOWARDPEEBLES PN A THEORETICAL-MODEL FOR UNAFFECTED CARRIER MALES IN FRAGILE-X FAMILIES | 0 | 0 |
| 199 | 0 | 0 | 199 1984 CLINICAL RESEARCH 32(5):A885-A885 HOLMAN GH; ALLEN SM; TUCKER DA; TAWATER BA SEIZURES AND UNUSUAL VISUAL EVOKED-RESPONSES IN FRAGILE-X CARRIERS | 0 | 0 |
| 200 | 0 | 0 | 200 1984 CYTOGENETICS AND CELL GENETICS 37(1-4):432-432 CAMERINO G; MATTEI MG; MATTEI JF; JAYE M; MANDEL JL CLOSE LINKAGE BETWEEN THE LOCI FOR THE FRAGILE X MENTAL-RETARDATION AND HEMOPHILIA-B | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 201 | 0 | 0 | 201 1984 CYTOGENETICS AND CELL GENETICS 37(1-4):587-587 SNYDER FF; LIN CC; HARASYM CA; JAMRO HK; KUSHNIG ML; et al. EVIDENCE FOR CLOSE ASSOCIATION BETWEEN THE FRAGILE X(Q27-28)-CHROMOSOME SITE AND GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD) BUT NOT WITH HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE (HPRT) | 3 | 3 |
| 202 | 0 | 0 | 202 1984 EMERGENCY MEDICINE 16(15):103-& [Anon] IN SEARCH OF THE FRAGILE-X | 0 | 0 |
| 203 | 0 | 0 | 203 1984 EUROPEAN JOURNAL OF PEDIATRICS 141(4):265-265 LARGO RH; SCHINZEL A DEVELOPMENTAL AND BEHAVIORAL DISTURBANCES IN BOYS WITH THE FRAGILE-X SYNDROME | 1 | 4 |
| 204 | 0 | 9 | 204 1984 HUMAN GENETICS 65(4):400-401 FRYNS JP; KLECZKOWSKA A; KUBIEN E; PETIT P; VANDENBERGHE H INACTIVATION PATTERN OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS | 18 | 27 |
| 205 | 0 | 1 | 205 1984 HUMAN GENETICS 66(1):100-100 GARDNER RJM FRAGILE-X HOMOZYGOSITY DUE TO SOMATIC CROSSING-OVER | 1 | 2 |
| 206 | 3 | 24 | 206 1984 HUMAN GENETICS 67(1):99-102 CANTU ES; JACOBS PA FRAGILE (X) EXPRESSION - RELATIONSHIP TO THE CELL-CYCLE | 4 | 7 |
| 207 | 2 | 10 | 207 1984 HUMAN GENETICS 68(2):189-190 REIDY JA; CHEN ATL FOLIC-ACID AND CHROMOSOME BREAKAGE .2. A METHIONINE EFFECT SIMILAR TO THAT IN FRAGILE-X EXPRESSION | 1 | 9 |
| 208 | 3 | 6 | 208 1984 HUMAN GENETICS 68(4):346-347 DEARCE MA VERIFICATION OF LYONS HYPOTHESIS IN FRAGILE-X CARRIERS | 2 | 5 |
| 209 | 0 | 0 | 209 1984 IRISH JOURNAL OF MEDICAL SCIENCE 153(1):29-30 DEARCE MA; LAW E A SIMPLE STATISTICAL APPROACH TO AVOID FALSE POSITIVES IN THE CYTOGENETIC DIAGNOSIS OF FRAGILE X-CHROMOSOMES | 0 | 0 |
| 210 | 0 | 0 | 210 1984 JAPANESE JOURNAL OF GENETICS 59(6):618-619 HORI T; AYUSAWA D; SENO T EXPRESSION OF THE FRAGILE X-CHROMOSOME UNDER CONDITIONS OF THYMIDYLATE STRESS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 211 | 0 | 3 | 211 1984 JOURNAL DE GENETIQUE HUMAINE 32(3):193-197 CRIPPA L; DELOZIERBLANCHET CD; ENGEL E STUDIES OF THE CYTOGENETIC VARIATIONS OF THE FRAGILE-X (FRA-X) ACCORDING TO CASES AND METHODS | 0 | 3 |
| 212 | 7 | 8 | 212 1984 JOURNAL DE GENETIQUE HUMAINE 32(3):199-207 GILGENKRANTZ S; BOUE J; GREGOIRE MJ; TEJADA I MENTAL-RETARDATION AND (FRA-X) FRAGILE-X CHROMOSOME | 0 | 3 |
| 213 | 5 | 25 | 213 1984 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 14(2):197-204 AUGUST GJ; LOCKHART LH FAMILIAL AUTISM AND THE FRAGILE-X-CHROMOSOME | 10 | 21 |
| 214 | 2 | 6 | 214 1984 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 14(4):451-452 JACKSON A; HOGERMAN R; LEVITAS A SEROTONIN LEVELS IN FRAGILE-X AUTISTIC PATIENTS | 1 | 3 |
| 215 | 0 | 1 | 215 1984 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 5(3):160-161 DESPOSITO F THE FRAGILE X-SYNDROME - DIAGNOSIS, BIOCHEMISTRY AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 216 | 2 | 8 | 216 1984 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 5(4):201-203 KERBESHIAN J; BURD L; MARTSOLF JT FRAGILE X-SYNDROME ASSOCIATED WITH TOURETTE SYMPTOMATOLOGY IN A MALE WITH MODERATE MENTAL-RETARDATION AND AUTISM | 4 | 29 |
| 217 | 1 | 3 | 217 1984 JOURNAL OF MEDICAL GENETICS 21(1):74-75 SUTHERLAND GR ROUTINE DIAGNOSTIC-DETECTION OF THE FRAGILE X | 1 | 4 |
| 218 | 32 | 83 | 218 1984 JOURNAL OF MEDICAL GENETICS 21(2):84-91 DEARCE MA; KEARNS A THE FRAGILE X-SYNDROME - THE PATIENTS AND THEIR CHROMOSOMES | 9 | 20 |
| 219 | 0 | 0 | 219 1984 JOURNAL OF MEDICAL GENETICS 21(4):298-298 WEBB TP; BUNDEY SE; THAKE A; TODD J STUDY OF THE FRAGILE X-CHROMOSOME AND MENTAL-RETARDATION | 0 | 3 |
| 220 | 0 | 0 | 220 1984 JOURNAL OF MEDICAL GENETICS 21(4):299-299 PEMBREY ME; WINTER RM; DAVIES KE A PERMUTATION THAT GENERATES THE DEFINITIVE MUTATION BY RECOMBINATION EXPLAINS THE INHERITANCE OF THE MARTIN-BELL SYNDROME (FRAGILE-X) | 9 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 221 | 0 | 4 | 221 1984 JOURNAL OF MEDICAL GENETICS 21(5):373-373 FITCHETT M; SEABRIGHT M DELETED X-CHROMOSOMES IN PATIENTS WITH THE FRAGILE X-SYNDROME | 10 | 14 |
| 222 | 2 | 11 | 222 1984 JOURNAL OF NERVOUS AND MENTAL DISEASE 172(9):549-551 KERBESHIAN J; BURD L; MARTSOLF J A FAMILY WITH FRAGILE-X SYNDROME | 7 | 20 |
| 223 | 3 | 44 | 223 1984 JOURNAL OF SPEECH AND HEARING DISORDERS 49(3):328-332 PAUL R; COHEN DJ; BREG WR; WATSON M; HERMAN S FRAGILE-X SYNDROME - ITS RELATIONS TO SPEECH AND LANGUAGE DISORDERS | 13 | 17 |
| 224 | 1 | 4 | 224 1984 LANCET 1(8370):220-220 WEBB T; THAKE A; TODD J; BUNDEY S PREVALENCE OF FRAGILE X-CHROMOSOME | 2 | 4 |
| 225 | 2 | 4 | 225 1984 LANCET 1(8370):220-220 JANCAR J PREVALENCE OF FRAGILE X-CHROMOSOME | 1 | 3 |
| 226 | 0 | 4 | 226 1984 LANCET 1(8370):220-221 LINNA SL; SIMILA S; HARO E; HERVA R PREVALENCE OF FRAGILE X-CHROMOSOME | 2 | 4 |
| 227 | 1 | 2 | 227 1984 LANCET 2(8398):349-349 CHOO KH; GEORGE D; FILBY G; HALLIDAY JL; LEVERSHA M; et al. LINKAGE ANALYSIS OF X-LINKED MENTAL-RETARDATION WITH AND WITHOUT FRAGILE-X USING FACTOR-IX GENE PROBE | 22 | 44 |
| 228 | 6 | 11 | 228 1984 NEW ENGLAND JOURNAL OF MEDICINE 310(22):1462-1462 WATSON MS; LECKMAN JF; ANNEX B; BREG WR; BOLES D; et al. FRAGILE X IN A SURVEY OF 75 AUTISTIC MALES | 34 | 56 |
| 229 | 0 | 1 | 229 1984 NEW ENGLAND JOURNAL OF MEDICINE 310(22):1471-1471 STEIN M THE FRAGILE X SYNDROME - DIAGNOSIS, BIOCHEMISTRY, AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 230 | 3 | 11 | 230 1984 OBSTETRICS AND GYNECOLOGY 63(3):S19-S21 HOGGE WA; SCHONBERG SA; GLOVER TW; HECHT F; GOLBUS MS PRENATAL-DIAGNOSIS OF FRAGILE (X) SYNDROME | 7 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 231 | 0 | 0 | 231 1984 PATHOLOGY 16(1):108-108 SUTHERLAND GR THE FRAGILE X-CHROMOSOME | 0 | 0 |
| 232 | 0 | 0 | 232 1984 PATHOLOGY 16(1):108-108 THEOBALD TM; HAY DA INDIVIDUAL VARIATION AND SPECIFIC COGNITIVE DEFICITS IN THE FRAGILE X-SYNDROME | 0 | 0 |
| 233 | 3 | 23 | 233 1984 PEDIATRICS 74(5):883-886 CARMI R; MERYASH DL; WOOD J; GERALD PS FRAGILE-X SYNDROME ASCERTAINED BY THE PRESENCE OF MACRO-ORCHIDISM IN A 5-MONTH-OLD INFANT | 4 | 6 |
| 234 | 6 | 16 | 234 1984 PRENATAL DIAGNOSIS 4(1):61-66 WILSON MG; MARCHESE CA PRENATAL-DIAGNOSIS OF FRAGILE-X IN A HETEROZYGOUS FEMALE FETUS AND POSTNATAL FOLLOW-UP | 5 | 9 |
| 235 | 3 | 6 | 235 1984 PRENATAL DIAGNOSIS 4(6):473-474 VENTER PA; COETZEE DJ; BADENHORST A; MARX MP; HOF JO; et al. A CONFIRMED PRENATAL-DIAGNOSIS OF A FEMALE FETUS WITH THE FRAGILE X-CHROMOSOME | 1 | 4 |
| 236 | 3 | 35 | 236 1984 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES 81(24):7855-7859 SZABO P; PURRELLO M; ROCCHI M; ARCHIDIACONO N; ALHADEFF B; et al. CYTOLOGICAL MAPPING OF THE HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE GENE DISTAL TO THE FRAGILE-X SITE SUGGESTS A HIGH-RATE OF MEIOTIC RECOMBINATION ACROSS THIS SITE | 17 | 71 |
| 237 | 6 | 24 | 237 1984 SOMATIC CELL AND MOLECULAR GENETICS 10(4):409-413 WARREN ST; DAVIDSON RL EXPRESSION OF FRAGILE X-CHROMOSOME IN HUMAN RODENT SOMATIC-CELL HYBRIDS | 14 | 19 |
| 238 | 7 | 52 | 238 1985 ACTA NEUROPATHOLOGICA 67(3-4):289-295 RUDELLI RD; BROWN WT; WISNIEWSKI K; JENKINS EC; LAUREKAMIONOWSKA M; et al. ADULT FRAGILE X-SYNDROME - CLINICO-NEUROPATHOLOGIC FINDINGS | 77 | 116 |
| 239 | 3 | 7 | 239 1985 ACTA PAEDIATRICA SCANDINAVICA 74(6):974-974 FLOOD A; SANNER G REFRACTIVE ERRORS IN THE FRAGILE-X SYNDROME | 3 | 3 |
| 240 | 1 | 26 | 240 1985 AMERICAN JOURNAL OF DANCE THERAPY 8:67-80 WOLFSCHEIN EG; FISCH GS; COHEN IL A STUDY OF THE USE OF NONVERBAL SYSTEMS IN THE DIFFERENTIAL-DIAGNOSIS OF AUTISTIC, MENTALLY-RETARDED AND FRAGILE X-INDIVIDUALS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 241 | 9 | 24 | 241 1985 AMERICAN JOURNAL OF DISEASES OF CHILDREN 139(7):674-678 HAGERMAN R; KEMPER M; HUDSON M LEARNING-DISABILITIES AND ATTENTIONAL PROBLEMS IN BOYS WITH THE FRAGILE X-SYNDROME | 55 | 72 |
| 242 | 6 | 17 | 242 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(1):193-198 ABRUZZO MA; MAYER M; JACOBS PA THE EFFECT OF METHIONINE AND 5-AZACYTIDINE ON FRAGILE-X EXPRESSION | 3 | 5 |
| 243 | 8 | 29 | 243 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(3):463-472 MULLIGAN LM; PHILLIPS MA; FORSTERGIBSON CJ; BECKETT J; PARTINGTON MW; et al. GENETIC-MAPPING OF DNA SEGMENTS RELATIVE TO THE LOCUS FOR THE FRAGILE-X SYNDROME AT XQ27.3 | 6 | 49 |
| 244 | 11 | 29 | 244 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(3):543-552 ROSENBLATT DS; DUSCHENES EA; HELLSTROM FV; GOLICK MS; VEKEMANS MJJ; et al. FOLIC-ACID BLINDED TRIAL IN IDENTICAL-TWINS WITH FRAGILE-X SYNDROME | 9 | 13 |
| 245 | 4 | 18 | 245 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(5):947-955 CANTU ES; NUSSBAUM RL; AIRHART SD; LEDBETTER DH FRAGILE (X) EXPRESSION INDUCED BY FUDR IS TRANSIENT AND INVERSELY RELATED TO LEVELS OF THYMIDYLATE SYNTHASE ACTIVITY | 3 | 5 |
| 246 | 9 | 23 | 246 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(5):956-964 HOWARDPEEBLES PN; FRIEDMAN JM UNAFFECTED CARRIER MALES IN FAMILIES WITH FRAGILE-X SYNDROME | 14 | 19 |
| 247 | 2 | 28 | 247 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(6):1192-1205 NUSSBAUM RL; WALMSLEY RM; LESKO JG; AIRHART SD; LEDBETTER DH THYMIDYLATE SYNTHASE-DEFICIENT CHINESE-HAMSTER CELLS - A SELECTION SYSTEM FOR HUMAN-CHROMOSOME 18 AND EXPERIMENTAL SYSTEM FOR THE STUDY OF THYMIDYLATE SYNTHASE REGULATION AND FRAGILE-X EXPRESSION | 6 | 47 |
| 248 | 1 | 12 | 248 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 21(4):691-696 WANG JCC; BEARDSLEY GP; ERBE RW ANTIFOLATE-INDUCED MISINCORPORATION OF DEOXYURIDINE MONOPHOSPHATE INTO DNA BY CELLS FROM PATIENTS WITH THE FRAGILE-X SYNDROME | 2 | 5 |
| 249 | 12 | 32 | 249 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 21(4):709-717 PEMBREY ME; WINTER RM; DAVIES KE A PRE-MUTATION THAT GENERATES A DEFECT AT CROSSING OVER EXPLAINS THE INHERITANCE OF FRAGILE X MENTAL RETARDATION | 82 | 116 |
| 250 | 4 | 12 | 250 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 21(4):771-775 SHIMANUKI K; LIN MS; WILSON MG REDUCTION OF FRAGILE X-EXPRESSION IN BLOOD AFTER CRYOPRESERVATION | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 251 | 7 | 13 | 251 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 22(2):415-416 BARBI G; STEINBACH P FRAGILE-X AND MARTIN-BELL SYNDROME - NEW SOURCE OF INFORMATION | 1 | 3 |
| 252 | 7 | 19 | 252 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 22(3):571-575 MITCHELL JA; WRAY J; MICHALSKI K NEUROFIBROMATOSIS AND FRAGILE-X SYNDROME IN THE SAME PATIENT | 2 | 3 |
| 253 | 0 | 1 | 253 1985 AMERICAN JOURNAL OF MENTAL DEFICIENCY 89(4):448-448 CROCKER AC THE FRAGILE X-SYNDROME - DIAGNOSIS, BIOCHEMISTRY, AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 254 | 14 | 34 | 254 1985 AMERICAN JOURNAL OF MENTAL DEFICIENCY 90(2):119-123 DELACRUZ FF FRAGILE-X SYNDROME | 10 | 13 |
| 255 | 4 | 10 | 255 1985 AMERICAN JOURNAL OF PSYCHIATRY 142(1):108-110 GOLDFINE PE; MCPHERSON PM; HEATH GA; HARDESTY VA; BEAUREGARD LJ; et al. ASSOCIATION OF FRAGILE-X SYNDROME WITH AUTISM | 36 | 53 |
| 256 | 1 | 5 | 256 1985 AMERICAN JOURNAL OF PUBLIC HEALTH 75(7):715-716 MILUNSKY A AN IMPORTANT CLINICAL APPROACH IN DETECTING THE FRAGILE X-SYNDROME | 0 | 1 |
| 257 | 3 | 19 | 257 1985 AMERICAN JOURNAL OF PUBLIC HEALTH 75(7):771-772 TRUSLER S; BEATTYDESANA J FRAGILE X-SYNDROME - A PUBLIC-HEALTH CONCERN | 5 | 6 |
| 258 | 9 | 47 | 258 1985 ANNALS OF NEUROLOGY 18(6):665-669 WISNIEWSKI KE; FRENCH JH; FERNANDO S; BROWN WT; JENKINS EC; et al. FRAGILE X-SYNDROME - ASSOCIATED NEUROLOGICAL ABNORMALITIES AND DEVELOPMENTAL-DISABILITIES | 27 | 43 |
| 259 | 7 | 26 | 259 1985 ARCHIVES OF DISEASE IN CHILDHOOD 60(11):1001-1007 THAKE A; TODD J; BUNDEY S; WEBB T IS IT POSSIBLE TO MAKE A CLINICAL-DIAGNOSIS OF THE FRAGILE X-SYNDROME IN A BOY | 22 | 28 |
| 260 | 0 | 3 | 260 1985 CANADIAN MEDICAL ASSOCIATION JOURNAL 133(5):358-& SOUDEK D FRAGILE-X - A SYMPTOM OF THE DISEASE | 2 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 261 | 0 | 0 | 261 1985 CLINICAL CHEMISTRY 31(6):1008-1009 THIBODEAU SN; FAULK KR; SMITH AC; BERRY R; HAGERMAN R THE USE OF RECOMBINANT DNA TECHNIQUES TO DOCUMENT THE TRANSMISSION OF FRAGILE-X SYNDROME THROUGH AN UNAFFECTED MALE CARRIER | 0 | 0 |
| 262 | 7 | 27 | 262 1985 CLINICAL GENETICS 27(2):113-117 BLOMQUIST HK; BOHMAN M; EDVINSSON SO; GILLBERG C; GUSTAVSON KH; et al. FREQUENCY OF THE FRAGILE X-SYNDROME IN INFANTILE-AUTISM - A SWEDISH MULTICENTER STUDY | 51 | 85 |
| 263 | 2 | 8 | 263 1985 CLINICAL GENETICS 27(2):118-121 HIRTH L; SINGH S; SCHILLING S; MULLER E; GOEDDE HW DERMATOGLYPHIC FINDINGS IN PATIENTS WITH FRAGILE X-CHROMOSOME | 2 | 6 |
| 264 | 0 | 0 | 264 1985 CLINICAL GENETICS 27(3):307-307 FRYNS JP THE FRAGILE-X SYNDROME - A STUDY OF 83 INDEX-PATIENTS AND THEIR FAMILIES | 0 | 1 |
| 265 | 0 | 0 | 265 1985 CLINICAL GENETICS 27(3):334-335 SCHMIDT A PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME | 2 | 4 |
| 266 | 6 | 18 | 266 1985 CLINICAL GENETICS 27(5):463-467 GUSTAVSON KH; DAHLBOM K; FLOOD A; HOLMGREN G; BLOMQUIST HK; et al. EFFECT OF FOLIC-ACID TREATMENT IN THE FRAGILE X-SYNDROME | 10 | 14 |
| 267 | 4 | 8 | 267 1985 CLINICAL GENETICS 27(5):520-521 WEBB GC DETECTION OF THE FRAGILE X-CHROMOSOME AND OTHER FRAGILE SITES | 5 | 6 |
| 268 | 5 | 14 | 268 1985 CLINICAL GENETICS 27(6):529-534 WEBB TP CO-CULTIVATION STUDIES IN THE EXPRESSION OF FRAGILE(X) (Q27) IN LYMPHOCYTES | 1 | 2 |
| 269 | 4 | 11 | 269 1985 CLINICAL GENETICS 28(2):97-99 ABUELO D; CASTREE K; PUESCHEL S; PADREMENDOZA T; ZOLNIERZ K FREQUENCY OF FRAGILE X-CHROMOSOME IN NORMAL FEMALES | 2 | 5 |
| 270 | 3 | 6 | 270 1985 CLINICAL GENETICS 28(5):399-400 SOUDEK D DECREASE OF FRAGILE X-FREQUENCY IN STORED-BLOOD SAMPLES - INDIVIDUAL VARIABILITY | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 271 | 0 | 0 | 271 1985 CLINICAL GENETICS 28(5):422-423 DAVIES KE; OLD J; MCGLADE S; SPEER A; COUTELLE C; et al. LINKAGE OF RFLPS AROUND THE DMD AND BMD LOCI AND THE FRAGILE X-LOCUS | 0 | 0 |
| 272 | 0 | 0 | 272 1985 CLINICAL GENETICS 28(5):449-449 MAVROU A; SYRROU M; TSENGHI C; AGELAKIS M; YOUROUKOS S; et al. FRAGILE X-SYNDROME AND MENTAL-RETARDATION IN GREECE | 0 | 0 |
| 273 | 2 | 5 | 273 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):606-606 CONNOR JM; COLGAN JM; CROSSLEY JA; IMRIE SJ; YATES JRW; et al. MULTIPOINT LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE X-SYNDROME AND FAMILIES WITH HEMOPHILIA-B | 0 | 0 |
| 274 | 1 | 5 | 274 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):612-612 DAVIES KE; HARPER K; MATTEI MG; MATTEI JF; VEENEMA H; et al. LINKAGE RELATIONSHIP OF DNA SEGMENT 52A (HGM7-DXS51) AND FACTOR-IX (HGM7-F9) TO FRAGILE-X MENTAL-RETARDATION (FRAXQ27) | 0 | 0 |
| 275 | 0 | 0 | 275 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):645-645 GOONEWARDENA P; TOLUN A; GUSTAVSON KH; HOLMGREN G; LINDSTEN J; et al. STUDIES ON THE FRAGILE-X MENTAL-RETARDATION SYNDROME, DUCHENNE MUSCULAR-DYSTROPHY AND X-LINKED RETINITIS PIGMENTOSA IN SWEDISH FAMILIES, BY THE USE OF DNA PROBES | 0 | 0 |
| 276 | 0 | 5 | 276 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):653-653 HOLDEN JJA; MULLIGAN LM; FORSTERGIBSON C; SIMPSON NE; WHITE BN; et al. APPLICATION OF FLANKING DNA PROBES TO CARRIER DETECTION IN THE FRAGILE-X SYNDROME | 0 | 2 |
| 277 | 0 | 0 | 277 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):715-715 OBERLE I; ARVEILER B; MATTEI MG; MATTEI JF; BOUE J; et al. LINKAGE ANALYSIS OF THE FRAGILE X-MENTAL RETARDATION SYNDROME WITH FLANKING POLYMORPHIC DNA MARKERS | 2 | 5 |
| 278 | 0 | 4 | 278 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):726-726 PURRELLO M; ALHADEFF B; ROCCHI M; ARCHIDIACONO N; DRAYNA D; et al. RELATIVE POSITIVE OF POLYMORPHIC DNA LOCI OF THE HUMAN X-CHROMOSOME LONG ARM SUBTELOMERIC REGION WITH RESPECT TO THE FRAGILE X SITE (FRAXQ27) | 1 | 4 |
| 279 | 1 | 2 | 279 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):788-788 ZOLL B; ARNEMANN J; KRAWCZAK M; COOPER DN; PESCIA G; et al. THE LOCI FOR FRAGILE X-MENTAL RETARDATION SYNDROME AND COAGULATION FACTOR-IX ARE NOT CLOSELY LINKED | 0 | 0 |
| 280 | 0 | 0 | 280 1985 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 27(1):95-96 PUESCHEL SM; FINELLI PV NEUROLOGICAL INVESTIGATIONS IN PATIENTS WITH FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 281 | 9 | 44 | 281 1985 DISEASE MARKERS 3(1):9-25 JACOBS PA; SHERMAN SL THE FRAGILE(X) - A MARKER FOR THE MARTIN-BELL SYNDROME | 6 | 8 |
| 282 | 9 | 34 | 282 1985 EUROPEAN JOURNAL OF PEDIATRICS 143(4):269-275 LARGO RH; SCHINZEL A DEVELOPMENTAL AND BEHAVIORAL DISTURBANCES IN 13 BOYS WITH FRAGILE X-SYNDROME | 26 | 37 |
| 283 | 14 | 32 | 283 1985 HELVETICA PAEDIATRICA ACTA 40(2-3):133-152 SCHINZEL A; LARGO RH THE FRAGILE X-SYNDROME (MARTIN-BELL SYNDROME) - CLINICAL AND CYTOGENETIC FINDINGS IN 16 PREPUBERTAL BOYS AND IN 4 OF THEIR 5 FAMILIES | 4 | 8 |
| 284 | 1 | 15 | 284 1985 HUMAN GENETICS 69(1):44-46 WARREN ST; GLOVER TW; DAVIDSON RL; JAGADEESWARAN P LINKAGE AND RECOMBINATION BETWEEN FRAGILE X-LINKED MENTAL-RETARDATION AND THE FACTOR-IX GENE | 20 | 37 |
| 285 | 1 | 9 | 285 1985 HUMAN GENETICS 69(3):206-208 MAYER M; ABRUZZO MA; JACOBS PA; YEE SC A CYTOGENETIC STUDY OF A POPULATION OF RETARDED FEMALES WITH SPECIAL REFERENCE TO THE FRAGILE (X) SYNDROME | 4 | 10 |
| 286 | 5 | 19 | 286 1985 HUMAN GENETICS 69(3):209-211 KRAWCZUN MS; JENKINS EC; BROWN WT ANALYSIS OF THE FRAGILE-X CHROMOSOME - LOCALIZATION AND DETECTION OF THE FRAGILE SITE IN HIGH-RESOLUTION PREPARATIONS | 20 | 33 |
| 287 | 13 | 28 | 287 1985 HUMAN GENETICS 69(3):218-223 VONKOSKULL H; AULA P; AMMALA P; NORDSTROM AM; RAPOLA J IMPROVED TECHNIQUE FOR THE EXPRESSION OF FRAGILE-X IN CULTURED AMNIOTIC-FLUID CELLS | 5 | 9 |
| 288 | 11 | 40 | 288 1985 HUMAN GENETICS 69(4):289-299 SHERMAN SL; JACOBS PA; MORTON NE; FROSTERISKENIUS U; HOWARDPEEBLES PN; et al. FURTHER SEGREGATION ANALYSIS OF THE FRAGILE-X SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES | 236 | 349 |
| 289 | 2 | 17 | 289 1985 HUMAN GENETICS 69(4):327-331 MATTEI MG; BAETEMAN MA; HEILIG R; OBERLE I; DAVIES K; et al. LOCALIZATION BY INSITU HYBRIDIZATION OF THE COAGULATION FACTOR-IX GENE AND OF 2 POLYMORPHIC DNA PROBES WITH RESPECT TO THE FRAGILE-X SITE | 8 | 49 |
| 290 | 17 | 40 | 290 1985 HUMAN GENETICS 71(1):11-18 BROWN WT; GROSS AC; CHAN CB; JENKINS EC GENETIC-LINKAGE HETEROGENEITY IN THE FRAGILE X-SYNDROME | 33 | 49 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 291 | 3 | 5 | 291 1985 HUMAN GENETICS 71(2):182-182 PEMBREY ME; WINTER RM FURTHER SEGREGATION ANALYSIS OF THE FRAGILE X-SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES | 1 | 1 |
| 292 | 2 | 3 | 292 1985 HUMAN GENETICS 71(2):183-183 SHERMAN SL; JACOBS PA; MORTON NE FURTHER SEGREGATION ANALYSIS OF THE FRAGILE X-SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES - REPLY | 1 | 1 |
| 293 | 5 | 24 | 293 1985 JAPANESE JOURNAL OF CANCER RESEARCH 76(10):977-983 HORI T; AYUSAWA D; GLOVER TW; SENO T EXPRESSION OF FRAGILE SITE ON THE HUMAN-X CHROMOSOME IN SOMATIC-CELL HYBRIDS BETWEEN HUMAN FRAGILE-X CELLS AND THYMIDYLATE SYNTHASE-NEGATIVE MOUSE MUTANT-CELLS | 3 | 18 |
| 294 | 0 | 0 | 294 1985 JAPANESE JOURNAL OF HUMAN GENETICS 30(2):150-150 IKEDA T; MIYAGI C; HIRAYAMA K FRAGILE X-SYNDROME - REPORT OF 2 FAMILIES AND CYTOGENETIC STUDIES | 0 | 0 |
| 295 | 5 | 17 | 295 1985 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 15(3):335-338 PUESCHEL SM; HERMAN R; GRODEN G SCREENING-CHILDREN WITH AUTISM FOR FRAGILE-X SYNDROME AND PHENYLKETONURIA | 15 | 25 |
| 296 | 6 | 28 | 296 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(2):87-90 VARLEY CK; HOLM VA; EREN MO COGNITIVE AND PSYCHIATRIC VARIABILITY IN 3 BROTHERS WITH FRAGILE X-SYNDROME | 10 | 13 |
| 297 | 2 | 2 | 297 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(5):322-322 KERBESHIAN J; BURD L; MARTSOLF JT THE MULTIPOTENTIAL OUTCOME OF FRAGILE X-SYNDROME | 1 | 1 |
| 298 | 0 | 3 | 298 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(5):322-322 LAWRENCE RJ THE MULTIPOTENTIAL OUTCOME OF FRAGILE X-SYNDROME | 0 | 0 |
| 299 | 3 | 15 | 299 1985 JOURNAL OF MEDICAL GENETICS 22(2):85-91 TUCKERMAN E; WEBB T; BUNDEY SE FREQUENCY AND REPLICATION STATUS OF THE FRAGILE-X, FRA(X)(Q27-28), IN A PAIR OF MONOZYGOTIC TWINS OF MARKEDLY DIFFERING INTELLIGENCE | 21 | 36 |
| 300 | 5 | 29 | 300 1985 JOURNAL OF MEDICAL GENETICS 22(4):258-266 BUNDEY S; WEBB TP; THAKE A; TODD J A COMMUNITY STUDY OF SEVERE MENTAL-RETARDATION IN THE WEST MIDLANDS AND THE IMPORTANCE OF THE FRAGILE X-CHROMOSOME IN ITS ETIOLOGY | 16 | 32 |