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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by year, source, volume, issue, page.
Page 9: 1 (1) 2 (101) 3 (201) 4 (301) 5 (401) 6 (501) 7 (601) 8 (701) 9 (801) 10 (901) 11 (1001) 12 (1101) 13 (1201) 14 (1301) 15 (1401) 16 (1501) 17 (1601) 18 (1701) 19 (1801) 20 (1901) 21 (2001) 22 (2101) 23 (2201) 24 (2301)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 801 | 13 | 25 | 801 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):374-377 VOELCKEL MA; PELLISSIER MC; PIQUET C; NGUYEN C; BOCCACCIO I; PHILIP N; MATTEI JF FRAGILE-X SYNDROME IN AN EXTENDED FAMILY WITH SPECIAL REFERENCE TO AN AFFECTED MALE WITH KLINEFELTER SYNDROME | 2 | 2 |
| 802 | 1 | 5 | 802 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):378-379 DOBKIN CS; DRISCOLL MC; FERRANDO C POLYMERASE CHAIN-REACTION DETECTION OF THE DDE-I POLYMORPHISM IN THE FACTOR-IX GENE FOR FRAGILE-X LINKAGE ANALYSIS | 0 | 3 |
| 803 | 4 | 15 | 803 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):380-383 PERGOLIZZI R; BROWN WT; GOONEWARDENA P; BHAN R; DOBKIN C; DAHL N; PETTERSSON U MOLECULAR CHARACTERIZATION OF A DNA PROBE, U6.2, LOCATED CLOSE TO THE FRAGILE-X LOCUS | 0 | 0 |
| 804 | 11 | 25 | 804 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):391-395 LAIRD CD POSSIBLE ERASURE OF THE IMPRINT ON A FRAGILE-X CHROMOSOME WHEN TRANSMITTED BY A MALE | 8 | 15 |
| 805 | 4 | 7 | 805 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):396-399 SHERMAN SL COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME - REQUEST FOR PARTICIPATION | 2 | 2 |
| 806 | 4 | 23 | 806 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):400-403 JACKY PB; AHUJA YR; ANYANEYEBOA K; BREG WR; CARPENTER NJ; FROSTERISKENIUS UG; FRYNS JP; GLOVER TW; GUSTAVSON KH; HOEGERMAN SF; HOLMGREN G; HOWARDPEEBLES PN; JENKINS EC; KRAWCZUN MS; NERI G; PETTIGREW A; SCHAAP T; SCHONBERG SA; SHAPIRO LR; SPINNER N; STEINBACH P; VIANNAMORGANTE AM; WATSON MS; WILMOT PL GUIDELINES FOR THE PREPARATION AND ANALYSIS OF THE FRAGILE-X CHROMOSOME IN LYMPHOCYTES | 31 | 44 |
| 807 | 7 | 16 | 807 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):404-407 FISCH GS; SILVERMAN W; JENKINS EC GENETIC AND OTHER FACTORS THAT CONTRIBUTE TO VARIABILITY IN CYTOGENETIC EXPRESSION IN FRAGILE-X MALES | 4 | 7 |
| 808 | 0 | 4 | 808 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):408-410 SHAPIRO LR; WILMOT PL; SHAPIRO DA; PETTERSEN IM; CASAMASSIMA AC CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME - EFFICIENCY, UTILIZATION, AND TRENDS | 3 | 3 |
| 809 | 1 | 7 | 809 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):416-417 JENKINS LS; GRUENERT DC; JENKINS EC; SCHONBERG SA TRANSFORMATION AND ESTABLISHMENT OF FRAGILE-X CELL-LINES FROM AMNIOCYTES | 1 | 1 |
| 810 | 4 | 16 | 810 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):418-420 LEDBETTER SA; SCHWARTZ CE; DAVIES KE; LEDBETTER DH NEW SOMATIC-CELL HYBRIDS FOR PHYSICAL MAPPING IN DISTAL XQ AND THE FRAGILE-X REGION | 0 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 811 | 12 | 22 | 811 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):421-424 ROSENBERG C; VIANNAMORGANTE AM; OTTO PA; NAVAJAS L EFFECT OF X-INACTIVATION ON FRAGILE-X FREQUENCY AND MENTAL-RETARDATION | 3 | 5 |
| 812 | 6 | 20 | 812 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):429-433 KIMCHISARFATY C; GOITEIN R; KEREM B; WERNER M; MEIDAN B; SCHAAP T ENDOREDUPLICATION AND POLYPLOIDY IN FRAGILE-X CELLS INDUCED BY METHOTREXATE AND FLUORODEOXYURIDINE - IMPLICATIONS FOR DIAGNOSIS | 1 | 3 |
| 813 | 10 | 28 | 813 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):440-444 KUPKE KG; SORENG AL; MULLER U ORIGIN OF THE SUPERNUMERARY X-CHROMOSOME IN A PATIENT WITH FRAGILE-X AND KLINEFELTER SYNDROME | 7 | 9 |
| 814 | 2 | 4 | 814 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):445-446 HOWARDPEEBLES PN FRAGILE-X EXPRESSION - USE OF A DOUBLE INDUCTION SYSTEM | 2 | 4 |
| 815 | 4 | 11 | 815 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):453-455 SHAPIRO LR; WILMOT PL; MURPHY PD PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME - POSSIBLE END OF THE EXPERIMENTAL PHASE FOR AMNIOTIC-FLUID | 5 | 6 |
| 816 | 2 | 33 | 816 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):456-463 KRAWCZUN MS; JENKINS EC; DUNCAN CJ; STARKHOUCK SL; KUNAPORN S; SCHWARTZRICHSTEIN C; HONG G; BROWN WT DISTRIBUTION OF AUTOSOMAL FRAGILE SITES IN SPECIMENS CULTURED FOR PRENATAL FRAGILE-X DIAGNOSIS | 1 | 1 |
| 817 | 1 | 8 | 817 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):464-466 JENKINS EC; BROOKS SE; STARKHOUCK SL; DUNCAN CJ; BROOKS SLS; BROWN WT SV40-TRANSFORMED FRAGILE(X) AMNIOCYTES | 1 | 1 |
| 818 | 9 | 34 | 818 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):481-487 FISCH GS; ARINAMI T; FROSTERISKENIUS U; FRYNS JP; CURFS LM; BORGHGRAEF M; HOWARDPEEBLES PN; SCHWARTZ CE; SIMENSEN RJ; SHAPIRO LR RELATIONSHIP BETWEEN AGE AND IQ AMONG FRAGILE-X MALES - A MULTICENTER STUDY | 13 | 14 |
| 819 | 6 | 20 | 819 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):488-492 DEVONFLINDT R; BYBEL B; CHUDLEY AE; LOPES F SHORT-TERM-MEMORY AND COGNITIVE VARIABILITY IN ADULT FRAGILE-X FEMALES | 6 | 8 |
| 820 | 3 | 21 | 820 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):493-497 SUDHALTER V; SCARBOROUGH HS; COHEN IL SYNTACTIC DELAY AND PRAGMATIC DEVIANCE IN THE LANGUAGE OF FRAGILE-X MALES | 21 | 29 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 821 | 3 | 19 | 821 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):498-502 COHEN IL; VIETZE PM; SUDHALTER V; JENKINS EC; BROWN WT EFFECTS OF AGE AND COMMUNICATION LEVEL ON EYE CONTACT IN FRAGILE-X MALES AND NON-FRAGILE-X AUTISTIC MALES | 22 | 33 |
| 822 | 7 | 15 | 822 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):503-504 CRONISTER A; HAGERMAN RJ; WITTENBERGER M; AMIRI K MENTAL IMPAIRMENT IN CYTOGENETICALLY POSITIVE FRAGILE-X FEMALES | 14 | 15 |
| 823 | 7 | 12 | 823 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):505-508 BRAINARD SS; SCHREINER RA; HAGERMAN RJ COGNITIVE PROFILES OF THE CARRIER FRAGILE-X WOMAN | 20 | 24 |
| 824 | 3 | 9 | 824 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):509-509 HECHT F SEIZURE DISORDERS IN THE FRAGILE-X CHROMOSOME SYNDROME | 3 | 7 |
| 825 | 3 | 10 | 825 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):511-513 MUSUMECI SA; FERRI R; ELIA M; COLOGNOLA RM; BERGONZI P; TASSINARI CA EPILEPSY AND FRAGILE-X SYNDROME - A FOLLOW-UP-STUDY | 21 | 36 |
| 826 | 5 | 15 | 826 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 39(3):374-375 MOORE PSJ; CHUDLEY AE; WINTER JSD PITUITARY-GONADAL AXIS IN PREPUBERTAL BOYS WITH THE FRAGILE-X SYNDROME | 5 | 7 |
| 827 | 14 | 31 | 827 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(2):234-243 CIANCHETTI C; SANNIOFANCELLO G; FRATTA AL; MANCONI F; ORANO A; PISCHEDDA MP; PRUNA D; SPINICCI G; ARCHIDIACONO N; FILIPPI G NEUROPSYCHOLOGICAL, PSYCHIATRIC, AND PHYSICAL MANIFESTATIONS IN 149 MEMBERS FROM 18 FRAGILE-X FAMILIES | 16 | 19 |
| 828 | 2 | 4 | 828 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(4):523-523 DREESEN JCFM; SMITS A; BRUNNER H RISK CALCULATIONS IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 829 | 2 | 5 | 829 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(4):524-524 WILLEMS PJ; VANROY B; RAEYMAEKERS P; OOSTRA B RISK CALCULATIONS IN THE FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 830 | 2 | 12 | 830 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 41(3):275-278 LACHIEWICZ AM; HOEGERMAN SF; HOLMGREN G; HOLMBERG E; ARINBJARNARSON K ASSOCIATION OF THE ROBIN SEQUENCE WITH THE FRAGILE-X SYNDROME | 5 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 831 | 10 | 39 | 831 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 41(3):289-294 HINTON VJ; BROWN WT; WISNIEWSKI K; RUDELLI RD ANALYSIS OF NEOCORTEX IN 3 MALES WITH THE FRAGILE-X SYNDROME | 76 | 117 |
| 832 | 1 | 15 | 832 1991 ANNALES DE GENETIQUE 34(2):111-114 BARLETTA C; RAGUSA RM; GAROFALO G; SCILLATO F; RUGGERI M SEGREGATION ANALYSIS OF AUTOSOMAL FRAGILE SITES IN 3 FAMILIES WITH THE FRAGILE X-CHROMOSOME | 0 | 5 |
| 833 | 4 | 31 | 833 1991 ANNALS OF NEUROLOGY 29(1):26-32 REISS AL; AYLWARD E; FREUND LS; JOSHI PK; BRYAN RN NEUROANATOMY OF FRAGILE-X-SYNDROME - THE POSTERIOR-FOSSA | 54 | 110 |
| 834 | 0 | 0 | 834 1991 ANNALS OF NEUROLOGY 30(3):450-450 BERRYKRAVIS E; HODGES C DEMONSTRATION OF ABNORMAL CYCLIC ADENOSINE-MONOPHOSPHATE PRODUCTION IN MULTIPLE TISSUES FROM INDIVIDUALS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 835 | 16 | 38 | 835 1991 BIOESSAYS 13(5):243-251 JORDAN BR FRAGILE X-LINKED MENTAL-RETARDATION AND THE DIFFICULTIES OF REVERSE GENETICS | 1 | 1 |
| 836 | 5 | 13 | 836 1991 BIOLOGICAL PSYCHIATRY 29(3):298-299 MENDLEWICZ J; HIRSCH D BIPOLAR MANIC-DEPRESSIVE ILLNESS AND THE FRAGILE-X SYNDROME | 0 | 1 |
| 837 | 1 | 2 | 837 1991 BRITISH MEDICAL JOURNAL 302(6789):1359-1359 CHARATAN F GENE FOR FRAGILE-X SYNDROME DISCOVERED | 0 | 0 |
| 838 | 9 | 34 | 838 1991 CELL 64(4):861-866 BELL MV; HIRST MC; NAKAHORI Y; MACKINNON RN; ROCHE A; FLINT TJ; JACOBS PA; TOMMERUP N; TRANEBJAERG L; FROSTERISKENIUS U; KERR B; TURNER G; LINDENBAUM RH; WINTER R; PEMBREY M; THIBODEAU S; DAVIES KE PHYSICAL MAPPING ACROSS THE FRAGILE-X - HYPERMETHYLATION AND CLINICAL EXPRESSION OF THE FRAGILE-X SYNDROME | 118 | 222 |
| 839 | 11 | 40 | 839 1991 CELL 65(5):905-914 VERKERK AJMH; PIERETTI M; SUTCLIFFE JS; FU YH; KUHL DPA; PIZZUTI A; REINER O; RICHARDS S; VICTORIA MF; ZHANG FP; EUSSEN BE; VANOMMEN GJB; BLONDEN LAJ; RIGGINS GJ; CHASTAIN JL; KUNST CB; GALJAARD H; CASKEY CT; NELSON DL; OOSTRA BA; WARREN ST IDENTIFICATION OF A GENE (FMR-1) CONTAINING A CGG REPEAT COINCIDENT WITH A BREAKPOINT CLUSTER REGION EXHIBITING LENGTH VARIATION IN FRAGILE-X SYNDROME | 501 | 1246 |
| 840 | 10 | 15 | 840 1991 CELL 66(4):817-822 PIERETTI M; ZHANG FP; FU YH; WARREN ST; OOSTRA BA; CASKEY CT; NELSON DL ABSENCE OF EXPRESSION OF THE FMR-1 GENE IN FRAGILE-X SYNDROME | 291 | 583 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 841 | 12 | 23 | 841 1991 CELL 67(6):1047-1058 FU YH; KUHL DPA; PIZZUTI A; PIERETTI M; SUTCLIFFE JS; RICHARDS S; VERKERK AJMH; HOLDEN JJA; FENWICK RG; WARREN ST; OOSTRA BA; NELSON DL; CASKEY CT VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX | 368 | 933 |
| 842 | 5 | 10 | 842 1991 CLINICAL GENETICS 39(5):347-354 BUTLER MG; MANGRUM T; GUPTA R; SINGH DN A 15-ITEM CHECKLIST FOR SCREENING MENTALLY-RETARDED MALES FOR THE FRAGILE X-SYNDROME | 28 | 32 |
| 843 | 4 | 13 | 843 1991 CLINICAL PEDIATRICS 30(5):318-321 HO HH; EAVES LC; PAYNE E VARIABILITY OF DEVELOPMENT IN 3 SIBLINGS WITH FRAGILE-X SYNDROME | 0 | 1 |
| 844 | 0 | 0 | 844 1991 CLINICAL RESEARCH 39(1):A1-A1 GOLDSON E; HAGERMAN RJ TEMPERAMENT AND THE FRAGILE-X SYNDROME | 2 | 2 |
| 845 | 0 | 0 | 845 1991 CLINICAL RESEARCH 39(3):A722-A722 BERRYKRAVIS E; HODGES C DEFECTIVE CYCLIC-AMP PRODUCTION IN TISSUES FROM PATIENTS WITH FRAGILE-X SYNDROME | 0 | 0 |
| 846 | 9 | 28 | 846 1991 COMPREHENSIVE PSYCHIATRY 32(1):83-87 TRANEBAERG L; ORUM A MAJOR DEPRESSIVE DISORDER AS A PROMINENT BUT UNDERESTIMATED FEATURE OF FRAGILE-X SYNDROME | 2 | 4 |
| 847 | 0 | 0 | 847 1991 CYTOGENETICS AND CELL GENETICS 56(3-4):221-221 SHAPIRO LR; EALLONARDO SJ; WILMOT PL INTERNAL CONTROL FOR SUCCESSFUL INDUCTION OF THE FRAGILE X-CHROMOSOME - OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION ELIMINATED | 1 | 1 |
| 848 | 0 | 2 | 848 1991 CYTOGENETICS AND CELL GENETICS 56(3-4):221-221 HOWARDPEEBLES PN FRAGILE X SCREENING VS FAMILY STUDIES (ESPECIALLY IN FEMALES) - LABORATORY PROCEDURES GUIDELINES | 0 | 0 |
| 849 | 2 | 9 | 849 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2054-2055 BOUVET A; BASRUR PK A MARKER FRAGILE X-CHROMOSOME ASSOCIATED WITH BALDY CALF SYNDROME | 0 | 1 |
| 850 | 0 | 0 | 850 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2062-2062 DJABALI M; NGUYEN C; BIUNNO I; IKEDA JE; OOSTRA BA; MATTEI MG; JORDAN BR LASER MICRODISSECTION OF THE FRAGILE-X REGION ALLOWS ISOLATION OF COSMID CLONES CONTAINING CONSERVED SEQUENCES | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 851 | 0 | 2 | 851 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2062-2062 DIETRICH A; LANGENSTEIN G; TONIOLO D; WARREN ST; LEHRACH H; POUSTKA A A PHYSICAL MAP OF THE HUMAN XQ27-QTER - LOCALIZING THE REGION OF THE FRAGILE-X MUTATION | 0 | 0 |
| 852 | 2 | 5 | 852 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2065-2065 GRAHAM CA; GRIER DG; CLARKSON M; STEWART FJ; NEVIN NC LINKAGE ANALYSIS IN FRAGILE-X SYNDROME | 0 | 0 |
| 853 | 2 | 5 | 853 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2067-2067 HIRST M; NAKAHORI Y; KNIGHT S; ROCHE A; RAUT C; RACK K; FLYNN G; BUCKLE V; BELL M; CLAUSSEN U; LUDECKE H; SENGER G; HORSTHEMKE B; HOLLAND J; BENTLEY D; SUPER M; DAVIES K A YAC CONTIG ACROSS THE FRAGILE-X REGION DERIVED FROM CHROMOSOME MICRODISSECTION MARKERS | 0 | 0 |
| 854 | 0 | 0 | 854 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2076-2076 LYNCH M; KREMER EJ; PRITCHARD MA; YU S; BAKER E; NAGARAJA R; HEITZ D; HYLAND VJ; LITTLE RD; WADA M; TONIOLO D; VINCENT A; ROUSSEAU F; NANCARROW J; HOLMAN K; MULLEY JC; WARREN ST; MANDEL J; SCHLESSINGER D; SUTHERLAND GR; RICHARDS RI THE FRAGILE-X GENOTYPE IS CHARACTERIZED BY AN UNSTABLE REGION OF DNA | 0 | 0 |
| 855 | 0 | 4 | 855 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2082-2082 POUSTKA A; DIETRICH A; KIOSCHIS P; KORN B; GROSS B; MONACO A; TONIOLO D; WARREN S; LEHRACH H MOLECULAR CHARACTERIZATION OF THE FRAGILE-X REGION | 0 | 0 |
| 856 | 1 | 3 | 856 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2085-2085 RIGGINS GJ; SHERMAN SL; OOSTRA BA; FEITELL D; SUTCLIFFE JS; NELSON DL; VANOOST BA; SMITS AP; KUHL D; CASKEY CT; WARREN ST A HIGHLY POLYMORPHIC DINUCLEOTIDE REPEAT, DXS 548, IS TIGHTLY LINKED TO THE FRAGILE-X SITE | 1 | 2 |
| 857 | 12 | 47 | 857 1991 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 33(9):776-788 FERRIER LJ; BASHIR AS; MERYASH DL; JOHNSTON J; WOLFF P CONVERSATIONAL SKILLS OF INDIVIDUALS WITH FRAGILE-X SYNDROME - A COMPARISON WITH AUTISM AND DOWN-SYNDROME | 18 | 22 |
| 858 | 18 | 35 | 858 1991 GENOMICS 10(3):576-582 SUTHERS GK; MULLEY JC; VOELCKEL MA; DAHL N; VAISANEN ML; STEINBACH P; GLASS IA; SCHWARTZ CE; VANOOST BA; THIBODEAU SN; HAITES NE; OOSTRA BA; SCHINZEL A; CARBALLO M; MORRIS CP; HOPWOOD JJ; SUTHERLAND GR LINKAGE HOMOGENEITY NEAR THE FRAGILE-X LOCUS IN NORMAL AND FRAGILE-X FAMILIES | 9 | 13 |
| 859 | 9 | 23 | 859 1991 GENOMICS 10(4):1053-1060 DJABALI M; NGUYEN C; BIUNNO I; OOSTRA BA; MATTEI MG; IKEDA JE; JORDAN BR LASER MICRODISSECTION OF THE FRAGILE X REGION - IDENTIFICATION OF COSMID CLONES AND OF CONSERVED SEQUENCES IN THIS REGION | 1 | 25 |
| 860 | 2 | 8 | 860 1991 HUMAN GENETICS 87(1):95-96 KAHKONEN M; HAATAJA R; LEISTI J URIDINE ENHANCES EXPRESSION OF THE FRAGILE-X CHROMOSOME IN HUMAN-LYMPHOCYTES | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 861 | 7 | 16 | 861 1991 HUMAN GENETICS 87(3):369-372 HULSEBOS TJM; OOSTRA BA; BROERSEN S; SMITS A; VANOOST BA; WESTERVELD A NEW DISTAL MARKER CLOSELY LINKED TO THE FRAGILE-X LOCUS | 4 | 13 |
| 862 | 9 | 24 | 862 1991 HUMAN GENETICS 87(4):421-424 WOHRLE D; STEINBACH P FRAGILE-X EXPRESSION AND X-INACTIVATION .2. THE FRAGILE SITE AT XQ27.3 HAS A BASIC FUNCTION IN THE PATHOGENESIS OF FRAGILE X-LINKED MENTAL-RETARDATION | 6 | 8 |
| 863 | 5 | 10 | 863 1991 HUMAN GENETICS 87(4):503-505 STEEN AM; MARCUS S; SAHLEN S; NIELSEN KB; LAMBERT B THE FRAGILE-X MUTATION DOES NOT HAVE ANY MAJOR EFFECT ON THE EXPRESSION OF THE HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE (HPRT) LOCUS IN HUMAN FIBROBLASTS | 0 | 2 |
| 864 | 9 | 23 | 864 1991 JOURNAL OF ABNORMAL CHILD PSYCHOLOGY 19(3):253-262 EINFELD S; HALL W; LEVY F HYPERACTIVITY AND THE FRAGILE X SYNDROME | 11 | 12 |
| 865 | 6 | 28 | 865 1991 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 21(4):503-516 HODAPP RM; DYKENS EM; ORT SI; ZELINSKY DG; LECKMAN JF CHANGING PATTERNS OF INTELLECTUAL STRENGTHS AND WEAKNESSES IN MALES WITH FRAGILE-X SYNDROME | 5 | 15 |
| 866 | 4 | 15 | 866 1991 JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY 11(6):398-399 COHEN IL; TSIOURIS JA; PFADT A EFFECTS OF LONG-ACTING PROPRANOLOL ON AGONISTIC AND STEREOTYPED BEHAVIORS IN A MAN WITH PERVASIVE DEVELOPMENTAL DISORDER AND FRAGILE-X SYNDROME - A DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY | 1 | 4 |
| 867 | 4 | 4 | 867 1991 JOURNAL OF MEDICAL GENETICS 28(5):358-358 WEBB T; BUNDEY S PREVALENCE OF FRAGILE X-SYNDROME | 5 | 8 |
| 868 | 0 | 0 | 868 1991 JOURNAL OF MEDICAL GENETICS 28(12):809-810 JACOBS PA THE FRAGILE-X SYNDROME | 6 | 10 |
| 869 | 6 | 9 | 869 1991 JOURNAL OF MEDICAL GENETICS 28(12):811-813 CONNOR JM CLONING OF THE GENE FOR THE FRAGILE-X SYNDROME - IMPLICATIONS FOR THE CLINICAL GENETICIST | 1 | 1 |
| 870 | 6 | 6 | 870 1991 JOURNAL OF MEDICAL GENETICS 28(12):814-817 WEBB T MOLECULAR-GENETICS OF FRAGILE-X - A CYTOGENETICS VIEWPOINT - REPORT OF THE 5TH INTERNATIONAL-SYMPOSIUM ON X-LINKED MENTAL-RETARDATION, STRASBOURG, FRANCE, 12 TO 16 AUGUST 1991 | 3 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 871 | 5 | 10 | 871 1991 JOURNAL OF MEDICAL GENETICS 28(12):818-823 RICHARDS RI; HOLMAN K; KOZMAN H; KREMER E; LYNCH M; PRITCHARD M; YU S; MULLEY J; SUTHERLAND GR FRAGILE-X SYNDROME - GENETIC LOCALIZATION BY LINKAGE MAPPING OF 2 MICROSATELLITE REPEATS FRAXAC1 AND FRAXAC2 WHICH IMMEDIATELY FLANK THE FRAGILE SITE | 52 | 100 |
| 872 | 11 | 17 | 872 1991 JOURNAL OF MEDICAL GENETICS 28(12):824-829 HIRST MC; NAKAHORI Y; KNIGHT SJL; SCHWARTZ C; THIBODEAU SN; ROCHE A; FLINT TJ; CONNOR JM; FRYNS JP; DAVIES KE GENOTYPE PREDICTION IN THE FRAGILE-X SYNDROME | 27 | 36 |
| 873 | 11 | 20 | 873 1991 JOURNAL OF MEDICAL GENETICS 28(12):830-836 ROUSSEAU F; HEITZ D; OBERLE I; MANDEL JL SELECTION IN BLOOD-CELLS FROM FEMALE CARRIERS OF THE FRAGILE-X SYNDROME - INVERSE CORRELATION BETWEEN AGE AND PROPORTION OF ACTIVE X-CHROMOSOMES CARRYING THE FULL MUTATION | 62 | 84 |
| 874 | 1 | 6 | 874 1991 JOURNAL OF MEDICAL GENETICS 28(12):837-839 GRIFFITHS MJ; STRACHAN MC A SINGLE LYMPHOCYTE CULTURE FOR FRAGILE-X INDUCTION AND PROMETAPHASE CHROMOSOME ANALYSIS | 0 | 0 |
| 875 | 2 | 8 | 875 1991 JOURNAL OF REPRODUCTION AND FERTILITY 91(1):203-206 TEWARI R; RAO SRV REPLICATION STATUS OF THE FRAGILE X-CHROMOSOME AND ITS IMPLICATIONS FOR REPRODUCTIVE-PERFORMANCE IN THE INDIAN MOLE RAT (NESOKIA-INDICA) | 0 | 0 |
| 876 | 24 | 53 | 876 1991 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 30(5):825-830 PIVEN J; GAYLE J; LANDA R; WZOREK M; FOLSTEIN S THE PREVALENCE OF FRAGILE-X IN A SAMPLE OF AUTISTIC INDIVIDUALS DIAGNOSED USING A STANDARDIZED INTERVIEW | 7 | 26 |
| 877 | 9 | 18 | 877 1991 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 30(5):831-834 HILTON DK; MARTIN CA; HEFFRON WM; HALL BD; JOHNSON GL IMIPRAMINE TREATMENT OF ADHD IN A FRAGILE-X CHILD | 4 | 9 |
| 878 | 5 | 9 | 878 1991 LANCET 338(8772):956-957 HIRST M; KNIGHT S; DAVIES K; CROSS G; OCRAFT K; RAEBURN S; HEEGER S; EUNPU D; JENKINS EC; LINDENBAUM R PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 29 | 35 |
| 879 | 4 | 6 | 879 1991 LANCET 338(8772):957-958 DOBKIN CS; DING XH; JENKINS EC; KRAWCZUN MS; BROWN WT; GOONEWARDENA P; WILLNER J; BENSON C; HEITZ D; ROUSSEAU F PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 22 | 24 |
| 880 | 0 | 0 | 880 1991 M S-MEDECINE SCIENCES 7(4):378-379 OBERLE I; MANDEL JL FRAGILE-X MENTAL-RETARDATION - VERY LOCALIZED GENOMIC IMPRINTING CLOSELY LINKED TO CLINICAL EXPRESSION | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 881 | 0 | 0 | 881 1991 M S-MEDECINE SCIENCES 7(6):637-639 ROUSSEAU F; HEITZ D; OBERLE I; MANDEL JL; KRETZ C THE FRAGILE X-SYNDROME - NEW SURPRISES | 0 | 0 |
| 882 | 11 | 14 | 882 1991 NATURE 349(6310):624-626 VINCENT A; HEITZ D; PETIT C; KRETZ C; OBERLE I; MANDEL JL ABNORMAL PATTERN DETECTED IN FRAGILE-X PATIENTS BY PULSED-FIELD GEL-ELECTROPHORESIS | 105 | 164 |
| 883 | 3 | 12 | 883 1991 NATURE 349(6312):742-743 CRAIG I HUMAN-GENETICS - METHYLATION AND THE FRAGILE-X | 1 | 5 |
| 884 | 7 | 11 | 884 1991 NATURE 351(6326):439-440 DAVIES K HUMAN-GENETICS - BREAKING THE FRAGILE-X | 2 | 7 |
| 885 | 15 | 28 | 885 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1673-1681 ROUSSEAU F; HEITZ D; BIANCALANA V; BLUMENFELD S; KRETZ C; BOUE J; TOMMERUP N; VANDERHAGEN C; DELOZIERBLANCHET C; CROQUETTE MF; GILGENKRANTZ S; JALBERT P; VOELCKEL MA; OBERLE I; MANDEL JL DIRECT DIAGNOSIS BY DNA ANALYSIS OF THE FRAGILE X-SYNDROME OF MENTAL-RETARDATION | 268 | 438 |
| 886 | 6 | 11 | 886 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1720-1722 SUTHERLAND GR; GEDEON A; KORNMAN L; DONNELLY A; BYARD RW; MULLEY JC; KREMER E; LYNCH M; PRITCHARD M; YU S; RICHARDS RI PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT DETECTION OF THE UNSTABLE DNA-SEQUENCE | 61 | 86 |
| 887 | 7 | 11 | 887 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1736-1738 SHAPIRO LR THE FRAGILE X-SYNDROME - A PECULIAR PATTERN OF INHERITANCE | 2 | 5 |
| 888 | 10 | 25 | 888 1991 NUCLEIC ACIDS RESEARCH 19(10):2567-2572 DIETRICH A; KIOSCHIS P; MONACO AP; GROSS B; KORN B; WILLIAMS SV; SHEER D; HEITZ D; OBERLE I; TONIOLO D; WARREN ST; LEHRACH H; POUSTKA A MOLECULAR-CLONING AND ANALYSIS OF THE FRAGILE X-REGION IN MAN | 23 | 45 |
| 889 | 9 | 25 | 889 1991 NUCLEIC ACIDS RESEARCH 19(12):3283-3288 HIRST MC; RACK K; NAKAHORI Y; ROCHE A; BELL MV; FLYNN G; CHRISTADOULOU Z; MACKINNON RN; FRANCIS M; LITTLER AJ; ANAND R; POUSTKA AM; LEHRACH H; SCHLESSINGER D; DURSO M; BUCKLE VJ; DAVIES KE A YAC CONTIG ACROSS THE FRAGILE X SITE DEFINES THE REGION OF FRAGILITY | 16 | 42 |
| 890 | 10 | 20 | 890 1991 NUCLEIC ACIDS RESEARCH 19(16):4355-4359 NAKAHORI Y; KNIGHT SJL; HOLLAND J; SCHWARTZ C; ROCHE A; TARLETON J; WONG S; FLINT TJ; FROSTERISKENIUS U; BENTLEY D; DAVIES KE; HIRST MC MOLECULAR HETEROGENEITY OF THE FRAGILE-X SYNDROME | 61 | 91 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 891 | 0 | 0 | 891 1991 OPTOMETRY AND VISION SCIENCE 68(8):634-640 MAINO DM; WESSON M; SCHLANGE D; CIBIS G; MAINO JH OPTOMETRIC FINDINGS IN THE FRAGILE X-SYNDROME | 5 | 9 |
| 892 | 0 | 0 | 892 1991 PEDIATRIC RESEARCH 29(4):A134-A134 SHAPIRO LR; EALLONARDO SJ; WILMOT PL OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION AND THE FRAGILE-X SYNDROME | 0 | 0 |
| 893 | 11 | 23 | 893 1991 PRENATAL DIAGNOSIS 11(5):333-338 WEBB T EXPRESSION OF FRAGILE-X IN A FEMALE FETUS DIAGNOSED AFTER CHORIONIC VILLUS SAMPLING | 3 | 4 |
| 894 | 12 | 37 | 894 1991 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 88(19):8302-8306 POUSTKA A; DIETRICH A; LANGENSTEIN G; TONIOLO D; WARREN ST; LEHRACH H PHYSICAL MAP OF HUMAN XQ27-QTER - LOCALIZING THE REGION OF THE FRAGILE-X MUTATION | 7 | 75 |
| 895 | 9 | 33 | 895 1991 SCIENCE 251(4998):1236-1239 HEITZ D; ROUSSEAU F; DEVYS D; SACCONE S; ABDERRAHIM H; LEPASLIER D; COHEN D; VINCENT A; TONIOLO D; DELLAVALLE G; JOHNSON S; SCHLESSINGER D; OBERLE I; MANDEL JL ISOLATION OF SEQUENCES THAT SPAN THE FRAGILE-X AND IDENTIFICATION OF A FRAGILE-X RELATED CPG ISLAND | 86 | 139 |
| 896 | 0 | 0 | 896 1991 SCIENCE 252(5009):1070-1070 HOFFMAN M UNRAVELING THE GENETICS OF FRAGILE X-SYNDROME | 2 | 4 |
| 897 | 18 | 37 | 897 1991 SCIENCE 252(5009):1097-1102 OBERLE I; ROUSSEAU F; HEITZ D; KRETZ C; DEVYS D; HANAUER A; BOUE J; BERTHEAS MF; MANDEL JL INSTABILITY OF A 550 BASE PAIR DNA SEGMENT AND ABNORMAL METHYLATION IN FRAGILE X-SYNDROME | 394 | 835 |
| 898 | 3 | 9 | 898 1991 SCIENCE 252(5009):1179-1181 YU S; PRITCHARD M; KREMER E; LYNCH M; NANCARROW J; BAKER E; HOLMAN K; MULLEY JC; WARREN ST; SCHLESSINGER D; SUTHERLAND GR; RICHARDS RI FRAGILE-X GENOTYPE CHARACTERIZED BY AN UNSTABLE REGION OF DNA | 274 | 537 |
| 899 | 5 | 13 | 899 1991 SCIENCE 252(5013):1711-1714 KREMER EJ; PRITCHARD M; LYNCH M; YU S; HOLMAN K; BAKER E; WARREN ST; SCHLESSINGER D; SUTHERLAND GR; RICHARDS RI MAPPING OF DNA INSTABILITY AT THE FRAGILE-X TO A TRINUCLEOTIDE REPEAT SEQUENCE P(CCG)N | 200 | 575 |
| 900 | 3 | 4 | 900 1991 SCIENCE 253(5027):1467-1467 HECHT F FRAGILE-X GENE | 0 | 0 |
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