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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by NCR.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1401 | 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 |
| 1402 | 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 |
| 1403 | 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 |
| 1404 | 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 |
| 1405 | 2 | 9 | 911 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):61-64 REISS AL; CIANCHETTI C; COHEN IL; DEVRIES B; HAGERMAN R; HINTON V; FROSTER U; LACHIEWICZ A; MAZZOCCO M; SOBESKY W; SUDHALTER V BRIEF SCREENING QUESTIONNAIRE FOR DETERMINING AFFECTED STATE IN FRAGILE-X SYNDROME - A CONSENSUS RECOMMENDATION | 2 | 3 |
| 1406 | 7 | 9 | 926 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):167-169 SHAPIRO LR; WILMOT PL; ANDREE LE PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X CHROMOSOME - FEASIBILITY AND SPEED OF INSITU CLONAL METHOD IN AMNIOTIC-FLUID CELL TISSUE-CULTURE | 0 | 0 |
| 1407 | 8 | 9 | 995 1992 JOURNAL OF MEDICAL GENETICS 29(12):919-920 TARLETON J; WONG S; SCHWARTZ C DIRECT ANALYSIS OF THE FMR-1 GENE PROVIDES AN EXPLANATION FOR AN EXCEPTIONAL CASE OF A FRAGILE-X NEGATIVE, MENTALLY-RETARDED MALE IN A FRAGILE-X FAMILY | 1 | 2 |
| 1408 | 7 | 9 | 1007 1992 NATURE GENETICS 1(4):237-238 CHAKRAVARTI A FRAGILE-X FOUNDER EFFECT | 15 | 32 |
| 1409 | 4 | 9 | 1019 1992 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 92(4):28-31 LASTOCHKINA NA; KUPRIYANOVA TA; PUCHINSKAYA LM; MARINCHEVA GS; GORKOVA SA THE CLINICOELECTROPHYSIOLOGICAL CHARACTERIZATION OF WOMEN, HETEROZYGOUS CARRIERS OF FRAGILE X-CHROMOSOME | 1 | 1 |
| 1410 | 4 | 9 | 1064 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 47(2):216-220 WIEGERS AM; CURFS LMG; VERMEER ELMH; FRYNS JP ADAPTIVE-BEHAVIOR IN THE FRAGILE X-SYNDROME - PROFILE AND DEVELOPMENT | 5 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1411 | 7 | 9 | 1120 1993 JOURNAL OF MEDICAL GENETICS 30(9):785-787 SUZUMORI K; YAMAUCHI M; SEKI N; KONDO I; HORI T PRENATAL-DIAGNOSIS OF A HYPERMETHYLATED FULL FRAGILE-X MUTATION IN CHORIONIC VILLI OF A MALE FETUS | 1 | 4 |
| 1412 | 6 | 9 | 1127 1993 LANCET 342(8878):1025-1026 WANG Q; GREEN E; BARNICOAT A; GARRETT D; MULLARKEY M; BOBROW M; MATHEW CG CYTOGENETIC VERSUS DNA DIAGNOSIS IN ROUTINE REFERRALS FOR FRAGILE-X SYNDROME | 15 | 22 |
| 1413 | 8 | 9 | 1157 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):315-316 BUTLER MG; PRATESI R; VNENCAKJONES CL MOLECULAR-GENETIC SCREENING IN CYTOGENETICALLY NORMAL MENTALLY-RETARDED MALES WITH MANIFESTATIONS OF FRAGILE-X-SYNDROME | 2 | 3 |
| 1414 | 1 | 9 | 1170 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):400-402 SCHWARTZ CE; DEAN J; HOWARDPEEBLES PN; BUGGE M; MIKKELSEN M; TOMMERUP N; HULL C; HAGERMAN R; HOLDEN JJA; STEVENSON RE OBSTETRICAL AND GYNECOLOGICAL COMPLICATIONS IN FRAGILE-X CARRIERS - A MULTICENTER STUDY | 50 | 84 |
| 1415 | 1 | 9 | 1298 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 59(4):526-526 SCHIANO CM; DEMB HB; BROWN WT LACK OF SIGNIFICANT ASSOCIATION BETWEEN SPINA-BIFIDA AND THE FRAGILE-X SYNDROME | 0 | 0 |
| 1416 | 5 | 9 | 1340 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):370-379 Holden JJA Workshop for family and friends .1. The fragile X gene and its mutations | 0 | 0 |
| 1417 | 5 | 9 | 1343 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):408-410 HowardPeebles PN; Maddalena A; Black SH; Levinson G; Bick DP; Schulman JD Fragile X screening in pediatric and obstetrical patients | 2 | 2 |
| 1418 | 2 | 9 | 1352 1995 GENETIC COUNSELING 6(3):207-210 ALEMBIK Y; DOTT B; STOLL C RETT-LIKE SYNDROME IN FRAGILE-X SYNDROME | 1 | 6 |
| 1419 | 8 | 9 | 1377 1995 LANCET 345(8958):1147-1148 WILLEMSEN R; MOHKAMSING S; DEVRIES B; DEVYS D; VANDENOUWELAND A; MANDEL JL; GALJAARD H; OOSTRA B RAPID ANTIBODY-TEST FOR FRAGILE-X SYNDROME | 73 | 94 |
| 1420 | 4 | 9 | 1430 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):319-322 Fisch GS; Carpenter N; Maddalena A; Tarleton J; JulienInalsingh C; Holden JJA Rater reliability of fragile X mutation size estimates: A multilaboratory analysis | 5 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1421 | 8 | 9 | 1522 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):221-223 Ponsot G Fragile X syndrome. Early recognition. | 0 | 0 |
| 1422 | 6 | 9 | 1523 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):224-226 Gerard CL; Guillotte E; Servel F; Barbeau M Assessment and remediation of communication disorders in children with fragile X syndrome | 0 | 0 |
| 1423 | 1 | 9 | 1576 1997 CLINICAL GENETICS 51(1):71-74 Behjati F; Mullarkey M; Bergbaum A; Berry AC; Docherty Z Chromosome deletion 17p11.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation | 0 | 5 |
| 1424 | 4 | 9 | 1728 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):281-285 Teisl JT; Reiss AL; Mazzocco MMM Maximizing the sensitivity of a screening questionnaire for determining fragile X at-risk status | 2 | 2 |
| 1425 | 3 | 9 | 1739 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):331-333 Wen GY; Jenkins EC; Goldberg EM; Genovese M; Brown WT; Wisniewski HM Ultrastructure of the fragile X chromosome: New observations on the fragile site | 0 | 3 |
| 1426 | 4 | 9 | 1861 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(5):516-517 Limprasert P; Jaruratanasirikul S; Vasiknanonte P Unilateral macroorchidism in fragile X syndrome | 2 | 2 |
| 1427 | 5 | 9 | 2110 2002 BRAIN & DEVELOPMENT 24(8):766-769 Incorpora G; Sorge G; Sorge A; Pavone L Epilepsy in fragile X syndrome | 2 | 2 |
| 1428 | 2 | 8 | 74 1982 LANCET 1(8263):100-100 BROWN WT; FRIEDMAN E; JENKINS EC; BROOKS J; WISNIEWSKI K; RAGUTHU S; FRENCH JH ASSOCIATION OF FRAGILE-X SYNDROME WITH AUTISM | 49 | 77 |
| 1429 | 2 | 8 | 75 1982 LANCET 1(8263):100-100 SUTHERLAND GR; JACKY PB PRENATAL-DIAGNOSIS OF FRAGILE-X CHROMOSOME | 6 | 13 |
| 1430 | 3 | 8 | 159 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1431 | 7 | 8 | 209 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 |
| 1432 | 2 | 8 | 213 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 |
| 1433 | 2 | 8 | 260 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 |
| 1434 | 4 | 8 | 264 1985 CLINICAL GENETICS 27(5):520-521 WEBB GC DETECTION OF THE FRAGILE X-CHROMOSOME AND OTHER FRAGILE SITES | 5 | 6 |
| 1435 | 2 | 8 | 321 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):179-187 SHELLHART WC; CASAMASSIMO PS; HAGERMAN RJ; BELANGER GK ORAL FINDINGS IN FRAGILE-X SYNDROME | 4 | 8 |
| 1436 | 2 | 8 | 523 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):231-236 SUTHERS GK; TURNER G; MULLEY JC CASE-REPORT - FRAGILE-X SYNDROME AND NEPHROGENIC DIABETES-INSIPIDUS | 1 | 2 |
| 1437 | 2 | 8 | 526 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):347-354 SHAPIRO LR; WILMOT PL; MURPHY PD; BREG WR EXPERIENCE WITH MULTIPLE APPROACHES TO THE PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME - AMNIOTIC-FLUID, CHORIONIC VILLI, FETAL BLOOD AND MOLECULAR METHODS | 12 | 19 |
| 1438 | 3 | 8 | 531 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):401-406 FRYNS JP; VANDENBERGHE H INACTIVATION PATTERN OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS | 7 | 11 |
| 1439 | 6 | 8 | 626 1989 ARCHIVES OF DISEASE IN CHILDHOOD 64(9):1223-1224 WINTER RM FRAGILE-X MENTAL-RETARDATION | 1 | 3 |
| 1440 | 1 | 8 | 787 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):288-289 ZHAO Y; SHEN Y; LIU Y; ZHANG JC; YE LZ; MA SW; LO WHY; WU GY; CHENG ZY; ZHANG XZ FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) IN CHINA | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1441 | 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 |
| 1442 | 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 |
| 1443 | 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 |
| 1444 | 6 | 8 | 948 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):355-360 SHERMAN SL; BARBI G; BRONDUMNIELSEN K; BROWN WT; CARPENTER NJ; CHUDLEY AE; FERRAZ OP; FERREIRA P; GUSTAVSON KH; HALLIDAY J; HOCKEY A; HOWARDPEEBLES PN; JENKINS E; KENNERKNECHT I; KAHKONEN M; LADAIQUE P; LEISTI J; MADDALENA A; MAZURCZAK T; MATTEI JF; MATTINA T; MCKINLEY MJ; MURPHY P; PELLISSIER MC; PURVISSMITH S; ROBINSON H; SCAPAGNINI U; SCHAAP T; SHAPIRO LR; SMITS APT; STEINBACH P; TURNER G; UCHIDA IA; VANOOST BA; VOELCKEL MA; WEAVER DD; WEBB T COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME - ONE-YEAR PROGRESS REPORT | 2 | 4 |
| 1445 | 7 | 8 | 993 1992 JOURNAL OF MEDICAL GENETICS 29(10):726-729 TARLETON J; WONG S; HEITZ D; SCHWARTZ C DIFFICULT DIAGNOSIS OF THE FRAGILE X-SYNDROME MADE POSSIBLE BY DIRECT DETECTION OF DNA MUTATIONS | 1 | 1 |
| 1446 | 1 | 8 | 1074 1993 BRITISH JOURNAL OF HAEMATOLOGY 85(2):415-416 VORST EJ; LEVENE NA; NISANI R; BERREBI A FRAGILE-X SYNDROME AND MYELODYSPLASIA DISCOVERED DURING PREGNANCY | 3 | 5 |
| 1447 | 5 | 8 | 1174 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):436-442 JENKINS EC; MORYS I; HENDERSON J; GENOVESE M; CARTER M; LI SY; HOUCK GE; DING XH; STARKHOUCK SL; DOBKIN CS; BROWN WT FRAGILE-X INDUCTION SYSTEMS IN CVS CULTURES - EFFECT ON CYTOGENETIC, PCR, AND GENOMIC SOUTHERN BLOT DNA ANALYSES OF THE FMR-1 GENE | 1 | 1 |
| 1448 | 7 | 8 | 1177 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):452-453 JENKINS EC; GENOVESE M; DUNCAN CJ; GU H; STARKHOUCK S; LI SY; HENDERSON J; MORYS I; BROWN WT OCCURRENCE OF ANEUPLOIDY FOR THE X-CHROMOSOME IN OVER 1,300 UNRELATED SPECIMENS SCREENED FOR THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1449 | 3 | 8 | 1234 1994 JOURNAL OF MEDICAL GENETICS 31(1):76-78 TEJADA MI; MORNET E; TIZZANO E; MOLINA M; BAIGET M; BOUE A IDENTIFICATION BY MOLECULAR DIAGNOSIS OF MOSAIC TURNERS-SYNDROME IN AN OBLIGATE CARRIER FEMALE FOR FRAGILE-X SYNDROME | 4 | 8 |
| 1450 | 4 | 8 | 1248 1994 MOLECULAR AND CELLULAR PROBES 8(2):177-180 CAO J; TARLETON J; BARBERIO D; DAVIDOW LS A SIMPLE FRAGILE-X PCR ASSAY WITH 7-DEAZAGUANINE-SUBSTITUTED DNA VISUALIZED BY ETHIDIUM-BROMIDE | 2 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1451 | 5 | 8 | 1588 1997 HOSPITAL PRACTICE 32(4):73-& Warren ST Trinucleotide repetition and fragile X syndrome | 3 | 5 |
| 1452 | 5 | 8 | 1687 1998 JOURNAL OF MEDICAL GENETICS 35(10):878-878 Jenkins T; Krause A Molecular evidence that fragile X syndrome occurs in the South African black population | 0 | 0 |
| 1453 | 3 | 8 | 1787 1999 GENETICS AND MOLECULAR BIOLOGY 22(2):169-172 Pena SDJ; Sturzeneker R Diagnosis of the fragile X syndrome in males using methylation-specific PCR of the FMR1 locus | 0 | 2 |
| 1454 | 8 | 8 | 1827 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):11-13 Sherman SL Premature ovarian failure among fragile X premutation carriers: Parent-of-origin effect? | 4 | 8 |
| 1455 | 6 | 8 | 1829 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):254-255 Vianna-Morgante AM; Costa SS Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X | 8 | 15 |
| 1456 | 5 | 8 | 1870 2000 AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE 30(1):86-88 Driscoll G; Clark J; Elakis G; Turner G Early menopause in a family carrying a fragile X premutation | 1 | 3 |
| 1457 | 6 | 8 | 2222 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 116A(1):99-100 Banes SL; Begleiter ML; Butler MG 45,X/46,XY mosaicism and fragile X syndrome | 0 | 0 |
| 1458 | 6 | 8 | 2365 2004 PRENATAL DIAGNOSIS 24(1):67-68 Delatycki MB; Sheffield LJ; Wake S; Cohen J Screening approach for Fragile X syndrome | 0 | 0 |
| 1459 | 1 | 7 | 22 1981 JOURNAL OF MENTAL DEFICIENCY RESEARCH 25(DEC):253-& RICHARDS BW; SYLVESTER PE; BROOKER C FRAGILE X-LINKED MENTAL-RETARDATION - THE MARTIN-BELL SYNDROME | 36 | 55 |
| 1460 | 1 | 7 | 29 1981 LYON MEDICAL 246(20):428-429 [Anon] MENTAL-RETARDATION DUE TO A FRAGILE X-CHROMOSOME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1461 | 1 | 7 | 30 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 |
| 1462 | 2 | 7 | 62 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 |
| 1463 | 1 | 7 | 81 1982 PEDIATRICS 69(5):668-669 RHOADS FA X-LINKED MENTAL-RETARDATION AND FRAGILE-X OR MARKER-X SYNDROME | 11 | 12 |
| 1464 | 3 | 7 | 236 1985 ACTA PAEDIATRICA SCANDINAVICA 74(6):974-974 FLOOD A; SANNER G REFRACTIVE ERRORS IN THE FRAGILE-X SYNDROME | 3 | 3 |
| 1465 | 2 | 7 | 304 1985 LANCET 1(8433):870-870 TOMMERUP N; SONDERGAARD F; TONNESEN T; KRISTENSEN M; ARVEILER B; SCHINZEL A 1ST TRIMESTER PRENATAL-DIAGNOSIS OF A MALE FETUS WITH FRAGILE-X | 20 | 31 |
| 1466 | 2 | 7 | 308 1985 PRENATAL DIAGNOSIS 5(3):229-231 ROCCHI M; PECILE V; ARCHIDIACONO N; MONNI G; DUMEZ Y; FILIPPI G PRENATAL-DIAGNOSIS OF THE FRAGILE-X IN MALE MONOZYGOTIC TWINS - DISCORDANT EXPRESSION OF THE FRAGILE SITE IN AMNIOCYTES | 5 | 10 |
| 1467 | 1 | 7 | 314 1986 AMERICAN JOURNAL OF DISEASES OF CHILDREN 140(4):327-328 HAGERMAN RJ FRAGILE-X SYNDROME AND LEARNING-DISABILITIES - REPLY | 1 | 1 |
| 1468 | 3 | 7 | 344 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):531-535 JENKINS EC; DUNCAN CJ; KRAWCZUN MS; BERNS LM; SANZ MM; BROWN WT FREQUENCY OF TRIRADIAL OR MULTIRADIAL CONFIGURATIONS IN FRAGILE-X IDENTIFICATION | 3 | 5 |
| 1469 | 2 | 7 | 374 1986 CLINICAL GENETICS 29(3):191-195 HECHT F; FRYNS JP; VLIETINCK RF; VANDENBERGHE H GENETIC-CONTROL OVER FRAGILE X-CHROMOSOME EXPRESSION | 9 | 10 |
| 1470 | 4 | 7 | 451 1987 HUMAN GENETICS 75(3):269-271 WINTER RM POPULATION-GENETICS IMPLICATIONS OF THE PREMUTATION HYPOTHESIS FOR THE GENERATION OF THE FRAGILE X-MENTAL RETARDATION GENE | 11 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1471 | 4 | 7 | 491 1987 PRENATAL DIAGNOSIS 7(3):197-202 SUTHERLAND GR; BAKER E; PURVISSMITH S; HOCKEY A; KRUMINS E; EICHENBAUM SZ PRENATAL-DIAGNOSIS OF THE FRAGILE-X USING THYMIDINE INDUCTION | 5 | 13 |
| 1472 | 1 | 7 | 535 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):443-450 NOLIN SL; JENKINS EC; BROWN WT; DOBKIN CS INSITU NICK TRANSLATION OF THE FRAGILE-X REGION | 1 | 2 |
| 1473 | 2 | 7 | 615 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(6):978-979 ARINAMI T BRAIN-STEM AUDITORY EVOKED-POTENTIALS IN THE FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 1474 | 6 | 7 | 645 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(3):473-476 BOLTON P; RUTTER M; BUTLER L; SUMMERS D FEMALES WITH AUTISM AND THE FRAGILE-X | 7 | 11 |
| 1475 | 5 | 7 | 703 1990 HUMAN GENETICS 85(1):141-142 SUTHERS GK; SUTHERLAND GR RECOMBINATION AND THE FRAGILE-X | 0 | 0 |
| 1476 | 3 | 7 | 713 1990 JOURNAL OF MENTAL DEFICIENCY RESEARCH 34:81-86 COLLACOTT RA; DUCKETT DP; MATHEWS D; WARRINGTON JS; YOUNG ID DOWNS-SYNDROME AND FRAGILE-X SYNDROME IN A SINGLE PATIENT | 0 | 0 |
| 1477 | 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 |
| 1478 | 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 |
| 1479 | 7 | 7 | 1078 1993 CLINICAL GENETICS 43(3):157-159 MORNET E; JOKIC M; BOGYO A; TEJADA I; DELUCHAT C; BOUE J; BOUE A AFFECTED SIBS WITH FRAGILE-X SYNDROME EXHIBIT AN AGE-DEPENDENT DECREASE IN THE SIZE OF THE FRAGILE-X FULL MUTATION | 5 | 8 |
| 1480 | 6 | 7 | 1122 1993 LANCET 341(8841):373-374 PALOMAKI GE; HADDOW JE IS IT TIME FOR POPULATION-BASED PRENATAL SCREENING FOR FRAGILE-X | 10 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1481 | 6 | 7 | 1126 1993 LANCET 342(8878):1004-1005 YOUNG ID DIAGNOSING FRAGILE-X SYNDROME | 1 | 1 |
| 1482 | 4 | 7 | 1165 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):370-373 STEYAERT J; DECRUYENAERE M; BORGHGRAEF M; FRYNS JP PERSONALITY PROFILE IN ADULT FEMALE FRAGILE-X CARRIERS - ASSESSED WITH THE MINNESOTA MULTIPHASIC PERSONALITY PROFILE (MMPI) | 3 | 8 |
| 1483 | 4 | 7 | 1171 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):403-404 SCHAAP C; FRYNS JP SEVERE PROGRESSIVE NEUROLOGICAL DISORDER ASSOCIATED WITH HYDROCEPHALUS IN A MAN WITH FRAGILE-X-SYNDROME | 1 | 2 |
| 1484 | 6 | 7 | 1210 1994 CLINICAL GENETICS 45(4):186-189 LOPEZPAJARES I; DELICADO A; PASCUALCASTROVIEJO I; LOPEZMARTIN V; MORENO F; GARCIAMARCOS JA FRAGILE-X SYNDROME WITH EXTRA MICROCHROMOSOME | 0 | 1 |
| 1485 | 4 | 7 | 1314 1995 BRAIN & DEVELOPMENT 17(5):323-323 KONDO I NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN JAPANESE MENTALLY-RETARDED MALES - COMMENT | 0 | 0 |
| 1486 | 0 | 7 | 1338 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):359-362 Lin JFH Introduction to fragile X syndrome for parents | 0 | 0 |
| 1487 | 3 | 7 | 1439 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):370-372 Partington MW; Moore DY; Turner GM Confirmation of early menopause in fragile X carriers | 23 | 42 |
| 1488 | 0 | 7 | 1442 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):378-381 Wingrove EJ; Norris J; Barton PL; Hagerman R Experiences and attitudes concerning genetic testing and insurance in a Colorado population: A survey of families diagnosed with fragile X syndrome | 0 | 8 |
| 1489 | 4 | 7 | 1659 1998 HUMAN GENETICS 102(1):54-56 Storm K; Handig I; Reyniers E; Oostra BA; Kooy RF; Willems PJ Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndrome | 0 | 1 |
| 1490 | 3 | 7 | 1743 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):350-351 Faradz SMH; Buckley M; Tang LP; Leigh D; Holden JJA Molecular screening for fragile X syndrome among Indonesian children with developmental disability | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1491 | 4 | 7 | 1985 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 100(2):156-161 Kjaer I; Hjalgrim H; Russell BG Cranial and hand skeleton in fragile X syndrome | 0 | 0 |
| 1492 | 0 | 7 | 2070 2001 REVISTA DE NEUROLOGIA 33:S77-S81 Safont-Tria NB Psychomotricity and fragile X syndrome | 0 | 0 |
| 1493 | 0 | 7 | 2071 2001 REVISTA DE NEUROLOGIA 33:S82-S87 Furgang R Language therapy in fragile X syndrome | 0 | 0 |
| 1494 | 6 | 7 | 2095 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 107(4):344-345 Vink GR; Froster UG Comparison of FMR1-protein expression in lymphocytes, methylation pattern in Southern blot analysis, and IQ values in three sisters with the fragile X syndrome | 0 | 1 |
| 1495 | 3 | 7 | 2267 2003 GENETIC TESTING 7(4):345-346 Adir V; Shahak E; Dar H; Borochowitz ZU Detection of X chromosome aneuploidy using Southern blot analysis during routine population-based screening for Fragile X syndrome | 0 | 0 |
| 1496 | 2 | 7 | 2369 2004 REVISTA DE NEUROLOGIA 38(1):7-11 Artigas-Pallares J; Brun-Gasca C Can the behavioural phenotype of Fragile X syndrome be attributed to mental retardation and to attention deficit hyperactivity disorder? | 0 | 0 |
| 1497 | 0 | 6 | 3 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 |
| 1498 | 2 | 6 | 61 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 |
| 1499 | 1 | 6 | 80 1982 NEW ENGLAND JOURNAL OF MEDICINE 306(25):1551-1552 POPOVICH B; VEKEMANS M; ROSENBLATT D; MONROE P FRAGILE-X | 17 | 21 |
| 1500 | 2 | 6 | 154 1983 NEW ENGLAND JOURNAL OF MEDICINE 308(5):285-286 HECHT F; GLOVER TW ANTIBIOTICS CONTAINING TRIMETHOPRIM AND THE FRAGILE X-CHROMOSOME | 4 | 6 |
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