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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 6: 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 |
|---|---|---|---|---|---|
| 501 | 0 | 0 | 501 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):20-21 KEREM B; GOITEIN R; SCHAAP T THE DISTRIBUTION OF FRAGILE-X CHROMOSOMES IN AMNIOTIC CELLS CULTURED BY THE INSITU TECHNIQUE | 1 | 1 |
| 502 | 0 | 0 | 502 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):21-21 LEDBETTER DH; LEDBETTER SA HIGH-LEVELS OF FRAGILE-X EXPRESSION IN NORMAL MALES INDUCED BY APHIDICOLIN | 0 | 0 |
| 503 | 0 | 0 | 503 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):22-22 LEISTI J; KAHKONEN M; HERVA R; WINQVIST R; UKKOLA L; HEINO R; VAISANEN ML; REKILA A; LINNA SL THE FRAGILE-X SYNDROME IN NORTHERN FINLAND - A GENEALOGIC STUDY | 0 | 0 |
| 504 | 0 | 0 | 504 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):22-23 OBERLE I; ARVEILER B; WOELFLIN A; HOFKER M; PEARSON P; MANDEL JL GENETIC AND PHYSICAL MAPPING OF THE FRAGILE-X REGION - .A. NEW POLYMORPHIC MARKERS .B. IS THE FRAGILE-X SITE A PREFERENTIAL BREAKPOINT IN CHROMOSOME REARRANGEMENTS | 0 | 0 |
| 505 | 0 | 0 | 505 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):23-24 RUDELLI R; MADRID R; BROWN WT FURTHER NEUROPATHOLOGICAL OBSERVATIONS IN ADULT FRAGILE-X | 0 | 0 |
| 506 | 0 | 0 | 506 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):25-25 TOMMERUP N; REINTOFT I; RESKENIELSEN E; BRONDUMNIELSEN K; MIKKELSEN M UNSUSPECTED PRENATAL-DIAGNOSIS OF THE FRAGILE-X | 0 | 1 |
| 507 | 0 | 0 | 507 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):26-26 TOMMERUP N; TRANEBJAERG L; TONNESEN T; KASTERN W; HANSEN H; DISSING J IDENTICAL EXPRESSION OF THE FRAGILE-X BUT DISCORDANT CLINICAL MANIFESTATIONS IN MONOZYGOTIC TWINS WITH MARTIN-BELL SYNDROME | 0 | 0 |
| 508 | 0 | 0 | 508 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):26-27 TURNER G; PARTINGTON MW; ROBINSON H; LATHAM M; KENNY J; VANDENBERK M; LAING S; THODE A THE PROS AND CONS OF PREVENTIVE SCREENING FOR THE FRAGILE (X) | 0 | 0 |
| 509 | 195 | 429 | 509 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):31-60 SPANO LM; OPITZ JM BIBLIOGRAPHY ON X-LINKED MENTAL-RETARDATION, THE FRAGILE-X AND RELATED SUBJECTS-IV (1988) | 0 | 1 |
| 510 | 0 | 18 | 510 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):77-82 PHELAN MC; STEVENSON RE; COLLINS JL; TRENT HE FRAGILE-X SYNDROME AND NEOPLASIA | 7 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 511 | 8 | 20 | 511 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):83-98 WALDSTEIN G; HAGERMAN R AORTIC HYPOPLASIA AND CARDIAC VALVULAR ABNORMALITIES IN A BOY WITH FRAGILE-X SYNDROME | 5 | 5 |
| 512 | 4 | 16 | 512 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):99-107 FILIPPI G; PECILE V; RINALDI A; SINISCALCO M FRAGILE-X MUTATION AND KLINEFELTER SYNDROME - A REAPPRAISAL | 9 | 13 |
| 513 | 4 | 9 | 513 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):109-113 FRYNS JP; VANDENBERGHE H THE CONCURRENCE OF KLINEFELTER SYNDROME AND FRAGILE-X SYNDROME | 14 | 17 |
| 514 | 5 | 22 | 514 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):115-121 WATSON MS; BREG WR; PAULS D; BROWN WT; CARROLL AJ; HOWARDPEEBLES PN; MERYASH D; SHAPIRO LR ANEUPLOIDY AND THE FRAGILE-X SYNDROME | 6 | 8 |
| 515 | 16 | 49 | 515 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):123-142 PROUTY LA; ROGERS RC; STEVENSON RE; DEAN JH; PALMER KK; SIMENSEN RJ; COSTON GN; SCHWARTZ CE FRAGILE-X SYNDROME - GROWTH, DEVELOPMENT, AND INTELLECTUAL FUNCTION | 28 | 36 |
| 516 | 3 | 9 | 516 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):143-147 NIELSEN KB GROWTH-PATTERN IN BOYS WITH FRAGILE-X | 3 | 3 |
| 517 | 3 | 4 | 517 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):165-168 BUTLER MG; ALLEN GA; SINGH DN; CARPENTER NJ; HALL BD PHOTOANTHROPOMETRIC ANALYSIS OF INDIVIDUALS WITH THE FRAGILE-X SYNDROME | 6 | 10 |
| 518 | 6 | 11 | 518 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):177-183 MILONE G; CONTI L; RIZZO R; SANFILIPPO S; SAMMITO V; ROMANO C A DERMATOGLYPHIC STUDY OF A GROUP OF SICILIAN CHILDREN WITH FRAGILE-X SYNDROME | 1 | 2 |
| 519 | 13 | 27 | 519 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):191-200 KEMPER MB; HAGERMAN RJ; ALTSHULSTARK D COGNITIVE PROFILES OF BOYS WITH THE FRAGILE-X SYNDROME | 55 | 73 |
| 520 | 1 | 3 | 520 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):201-205 BROWN WT; RUDELLI RD; WISNIEWSKI HM FRAGILE-X SYNDROME - NEUROPATHOLOGY CENTER | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 521 | 10 | 36 | 521 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):213-225 WOLFF PH; GARDNER J; LAPPEN J; PACCIA J; MERYASH D VARIABLE EXPRESSION OF THE FRAGILE-X SYNDROME IN HETEROZYGOUS FEMALES OF NORMAL INTELLIGENCE | 28 | 35 |
| 522 | 2 | 4 | 522 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):227-230 HOWARDPEEBLES PN; BROWN WT THE FRAGILE-X SYNDROME - VARIABILITY OF EXPRESSION IN CARRIER FEMALES | 3 | 4 |
| 523 | 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 |
| 524 | 1 | 2 | 524 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):237-238 EINFELD SL AUTISM AND THE FRAGILE-X SYNDROME | 4 | 6 |
| 525 | 11 | 14 | 525 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):337-345 PURVISSMITH SG; LAING S; SUTHERLAND GR; BAKER E PRENATAL-DIAGNOSIS OF THE FRAGILE-X - THE AUSTRALASIAN EXPERIENCE | 0 | 14 |
| 526 | 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 |
| 527 | 21 | 61 | 527 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):355-368 MCKINLEY MJ; KEARNEY LU; NICOLAIDES KH; GOSDEN CM; WEBB TP; FRYNS JP PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME BY PLACENTAL (CHORIONIC VILLI) BIOPSY CULTURE | 8 | 13 |
| 528 | 3 | 4 | 528 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):369-376 SANFILIPPO S; RAGUSA RM; SCILLATO F; RUGGERI M; NERI G FRAGILE-X EXPRESSION IN NORMAL AND MENTALLY-RETARDED SUBJECTS - EFFECT OF TREATMENT WITH AN ANTIFOLIC AGENT | 0 | 3 |
| 529 | 12 | 44 | 529 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):377-392 HAGERMAN RJ; MURPHY MA; WITTENBERGER MD A CONTROLLED TRIAL OF STIMULANT MEDICATION IN CHILDREN WITH THE FRAGILE-X SYNDROME | 23 | 49 |
| 530 | 16 | 23 | 530 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):393-399 FISCH GS; COHEN IL; GROSS AC; JENKINS V; JENKINS EC; BROWN WT FOLIC-ACID TREATMENT OF FRAGILE-X MALES - A FURTHER STUDY | 4 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 531 | 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 |
| 532 | 3 | 3 | 532 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):417-422 TOMMERUP N; LAING S; CHRISTENSEN IJ; TURNER G SCREENING FOR THE FRAGILE-X - HOW MANY CELLS SHOULD WE ANALYZE | 6 | 8 |
| 533 | 1 | 2 | 533 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):423-428 TURNER G; PARTINGTON MW FRAGILE(X) EXPRESSION, AGE AND THE DEGREE OF INTELLECTUAL HANDICAP IN THE MALE | 4 | 5 |
| 534 | 21 | 49 | 534 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):435-442 KRAWCZUN MS; JENKINS EC; BROWN WT; SILVERMAN WP FRAGILE-X EXPRESSION IN SHORT-TERM WHOLE-BLOOD CULTURES IS AFFECTED BY CELL-DENSITY | 2 | 3 |
| 535 | 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 |
| 536 | 1 | 3 | 536 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):455-457 HOWARDPEEBLES P; FROSTERISKENIUS U FRAGILE-X TESTING IN MOTHERS OF TRANSMITTING MALES | 0 | 1 |
| 537 | 2 | 13 | 537 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):459-471 THODE A; LAING S; PARTINGTON MW; TURNER G IS THERE A FRAGILE(X) NEGATIVE MARTIN-BELL SYNDROME | 2 | 6 |
| 538 | 14 | 27 | 538 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):531-542 SCHWARTZ CE; PHELAN MC; BRIGHTHARP C; PANCOAST I; HOWARDPEEBLES PN; THIBODEAU S; BROWN WT; JENKINS EC FRAGILE-X SYNDROME - LINKAGE ANALYSIS IN BLACK AND WHITE-POPULATIONS | 4 | 4 |
| 539 | 8 | 22 | 539 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):543-550 HEILIG R; OBERLE I; ARVEILER B; HANAUER A; VIDAUD M; MANDEL JL IMPROVED DNA MARKERS FOR EFFICIENT ANALYSIS OF FRAGILE-X FAMILIES | 11 | 33 |
| 540 | 12 | 22 | 540 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):551-566 BROWN WT; YE W; GROSS AC; CHAN CB; DOBKIN CS; JENKINS EC MULTIPOINT LINKAGE OF 9 ANONYMOUS PROBES TO HPRT, FACTOR-IX, AND FRAGILE-X | 8 | 25 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 541 | 5 | 13 | 541 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):567-580 MULLEY J; TURNER G; BAIN S; SUTHERLAND GR LINKAGE BETWEEN THE FRAGILE-X AND F9, DXS52 (ST14), DXS98 (4D-8) AND DXS105 (CX55.7) | 13 | 20 |
| 542 | 4 | 18 | 542 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):613-623 WARREN ST; ZHANG F; SUTCLIFFE JS; PETERS JF STRATEGY FOR MOLECULAR-CLONING OF THE FRAGILE-X SITE DNA | 7 | 12 |
| 543 | 3 | 4 | 543 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):625-631 SHERMAN SL; TURNER G; SHEFFIELD L; LAING S; ROBINSON H INVESTIGATION OF THE TWINNING RATE IN FAMILIES WITH THE FRAGILE-X SYNDROME | 6 | 8 |
| 544 | 4 | 5 | 544 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):633-639 SHERMAN SL; TURNER G; ROBINSON H; LAING S INVESTIGATION OF THE SEGREGATION OF THE FRAGILE-X MUTATION IN DAUGHTERS OF OBLIGATE CARRIER WOMEN | 5 | 7 |
| 545 | 7 | 16 | 545 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):641-654 SCHWARTZ CE; PHELAN MC; PULLIAM LH; WILKES G; VANNER LV; ALBIEZ KL; POTTS WA; ROGERS RC; SCHROER RJ; SAUL RA; PROUTY LA; DEAN JH; TAYLOR HA; STEVENSON RE FRAGILE-X SYNDROME - INCIDENCE, CLINICAL AND CYTOGENETIC FINDINGS IN THE BLACK AND WHITE-POPULATIONS OF SOUTH-CAROLINA | 12 | 15 |
| 546 | 32 | 50 | 546 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):655-663 FISCH GS; COHEN IL; JENKINS EC; BROWN WT SCREENING DEVELOPMENTALLY DISABLED MALE POPULATIONS FOR FRAGILE-X - THE EFFECT OF SAMPLE-SIZE | 17 | 21 |
| 547 | 6 | 10 | 547 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):665-672 NERI G; SANFILIPPO S; PAVONE L; MOLLICA F; BARBERI I; GIUFFRE L; ROMANO C; MATTINA T; CAMMARATA M; RAGUSA MG; SAMMITO V; VENTIMIGLIA G; MUSUMECI SA THE FRAGILE-X IN SICILY - AN EPIDEMIOLOGICAL SURVEY | 9 | 16 |
| 548 | 8 | 12 | 548 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):673-679 HOLMGREN G; BLOMQUIST HK; DRUGGE U; GUSTAVSON KH FRAGILE-X FAMILIES IN A NORTHERN SWEDISH COUNTY - A GENEALOGICAL STUDY DEMONSTRATING APPARENT PATERNAL TRANSMISSION FROM THE 18TH-CENTURY | 10 | 10 |
| 549 | 7 | 21 | 549 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):681-688 WARREN ST FRAGILE-X SYNDROME - A HYPOTHESIS REGARDING THE MOLECULAR MECHANISM OF THE PHENOTYPE | 5 | 6 |
| 550 | 2 | 5 | 550 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):693-696 LAIRD CD FRAGILE-X MUTATION PROPOSED TO BLOCK COMPLETE REACTIVATION IN FEMALES OF AN INACTIVE X-CHROMOSOME | 7 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 551 | 8 | 28 | 551 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):697-702 SHABTAI F; HART J; KLAR D; BICHACHO S; HALBRECHT I FRAGILE-X EXPRESSION IN MARTIN-BELL SYNDROME, INTELLECTUALLY NORMAL INDIVIDUALS, AND NEOPLASIA, INTERPRETED BY A VIRAL HYPOTHESIS | 2 | 3 |
| 552 | 2 | 17 | 552 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(2):407-414 REISS AL; PATEL S; KUMAR AJ; FREUND L PRELIMINARY COMMUNICATION - NEUROANATOMICAL VARIATIONS OF THE POSTERIOR-FOSSA IN MEN WITH THE FRAGILE-X (MARTIN-BELL) SYNDROME | 16 | 38 |
| 553 | 3 | 4 | 553 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):733-734 WILSON DP; CARPENTER NJ; BERKOVITZ G THYROID-FUNCTION IN MEN WITH FRAGILE X-LINKED MR | 3 | 3 |
| 554 | 8 | 13 | 554 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):735-739 MAVROU A; SYRROU M; TSENGHI C; AGELAKIS M; YOUROUKOS S; METAXOTOU C MARTIN-BELL SYNDROME IN GREECE, WITH REPORT OF ANOTHER 47,XXY FRAGILE X PATIENT | 7 | 10 |
| 555 | 5 | 12 | 555 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):753-765 SHERMAN SL; ROGATKO A; TURNER G RECURRENCE RISKS FOR RELATIVES IN FAMILIES WITH AN ISOLATED CASE OF THE FRAGILE X SYNDROME | 11 | 15 |
| 556 | 2 | 15 | 556 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):767-773 BUTLER MG; FLETCHER M; GALE DD; MEANEY FJ; MCLEOD DR; FAGAN J; CARPENTER NJ METACARPOPHALANGEAL PATTERN PROFILE ANALYSIS IN FRAGILE-X SYNDROME | 4 | 8 |
| 557 | 5 | 12 | 557 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):775-778 BUTLER MG; DEV VG; SHAH D; ULM JE; WILMOT PL; SHAPIRO LR THE USE OF EARLY SIMULTANEOUS PERCUTANEOUS UMBILICAL BLOOD-SAMPLING (PUBS) AND AMNIOCENTESIS FOR PRENATAL FRAGILE-X CHROMOSOME DIAGNOSIS | 0 | 0 |
| 558 | 2 | 10 | 558 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):779-781 BUTLER MG; NAJJAR JL DO SOME PATIENTS WITH FRAGILE-X SYNDROME HAVE PRECOCIOUS PUBERTY | 13 | 15 |
| 559 | 12 | 32 | 559 1988 AMERICAN JOURNAL ON MENTAL RETARDATION 92(5):436-446 COHEN IL; FISCH GS; SUDHALTER V; WOLFSCHEIN EG; HANSON D; HAGERMAN R; JENKINS EC; BROWN WT SOCIAL GAZE, SOCIAL AVOIDANCE, AND REPETITIVE BEHAVIOR IN FRAGILE X-MALES - A CONTROLLED-STUDY | 50 | 71 |
| 560 | 7 | 32 | 560 1988 ARCHIVES OF GENERAL PSYCHIATRY 45(1):25-30 REISS AL; HAGERMAN RJ; VINOGRADOV S; ABRAMS M; KING RJ PSYCHIATRIC DISABILITY IN FEMALE CARRIERS OF THE FRAGILE X-CHROMOSOME | 56 | 91 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 561 | 0 | 0 | 561 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):91-91 LAING S; LATHAM M; KENNY J; PURVISSMITH S; TURNER G CYTOGENETIC ANOMALIES IN A POPULATION SELECTED FOR FRAGILE-X SCREENING | 0 | 0 |
| 562 | 0 | 0 | 562 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):91-91 TURNER G ISSUES ARISING FROM FRAGILE-X PREVENTIVE SCREENING | 0 | 0 |
| 563 | 0 | 0 | 563 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):93-94 GARRY MB; MACFARLANE SC; PULLON DHH FRAGILE-X POSITIVE TURNERS MOSAIC | 0 | 0 |
| 564 | 0 | 0 | 564 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):96-96 PURVISSMITH S; LAING S; STEWART L; TURNER G; WASS D; SUTHERLAND G; LEVERSHA M PRENATAL-DIAGNOSIS OF FRAGILE-X | 0 | 0 |
| 565 | 0 | 2 | 565 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):97-97 SUTHERS GK; THODE A; TURNER GL CASE-REPORT - FRAGILE-X SYNDROME AND NEPHROGENIC DIABETES-INSIPIDUS | 0 | 0 |
| 566 | 4 | 44 | 566 1988 BRAIN AND LANGUAGE 34(2):203-221 VILKMAN E; NIEMI J; IKONEN U FRAGILE-X SPEECH PHONOLOGY IN FINNISH | 4 | 5 |
| 567 | 5 | 31 | 567 1988 CANCER 62(11):2383-2386 CUNNINGHAM M; DICKERMAN JD FRAGILE-X SYNDROME AND ACUTE LYMPHOBLASTIC-LEUKEMIA | 3 | 3 |
| 568 | 2 | 19 | 568 1988 CHROMOSOMA 96(5):391-396 SAVAGE JRK; FITCHETT M THE BEHAVIOR OF FRAGILE-X AND OTHER ABERRATIONS DURING RECOVERY FROM LOW FOLATE CONDITIONS | 0 | 3 |
| 569 | 2 | 29 | 569 1988 CHROMOSOMA 97(1):6-10 KEREM B; GOITEIN R; SCHAAP T CYTOLOGICAL EVIDENCE OF DEFECTIVE TEMPLATE IN THE FRAGILE X-CHROMOSOME | 2 | 5 |
| 570 | 6 | 13 | 570 1988 CLINICAL GENETICS 33(3):169-175 LOESCH DZ DISCRIMINANT-ANALYSIS OF DERMATOGLYPHIC MEASUREMENTS IN FRAGILE-X MALES AND FEMALES | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 571 | 1 | 13 | 571 1988 CLINICAL GENETICS 33(5):349-355 MERYASH DL; ABUELO D COUNSELING NEEDS AND ATTITUDES TOWARD PRENATAL-DIAGNOSIS AND ABORTION IN FRAGILE-X FAMILIES | 5 | 17 |
| 572 | 17 | 31 | 572 1988 CLINICAL GENETICS 33(6):410-417 VEENEMA H; BEVERSTOCK GC; DEKONING T; PEARSON PL; VANDEKAMP JJP THE FRAGILE X-CHROMOSOME - AN EVALUATION OF THE RESULTS IN A ROUTINE CYTOGENETIC LABORATORY IN THE PERIOD 1981-1986 | 1 | 3 |
| 573 | 0 | 0 | 573 1988 CLINICAL GENETICS 33(6):464-464 HULTEN M; JOHANNISSON R MEIOSIS IN THE FRAGILE-X MENTAL-RETARDATION SYNDROME | 0 | 0 |
| 574 | 7 | 21 | 574 1988 CLINICAL GENETICS 34(4):265-271 ANVRET M; GILLBERG C; WAHLSTROM J; ALBERTSSONWIKLAND K; DAVIES K INFANTILE-AUTISM, FRAGILE (X) (Q27.3) AND RFLP ANALYSIS IN AN EXTENDED SWEDISH FAMILY | 2 | 4 |
| 575 | 0 | 0 | 575 1988 CLINICAL RESEARCH 36(1):A207-A207 BIXENMAN H; HECHT F; LOCKWOOD D; HECHT BK NEW COMMON FRAGILE SITE AT XQ27.3 CONFOUNDED WITH FRAGILE-X | 0 | 0 |
| 576 | 7 | 32 | 576 1988 CYTOGENETICS AND CELL GENETICS 47(4):177-180 HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M FRAGILE-X EXPRESSION IN THYMIDINE-PROTOTROPHIC AND AUXOTROPHIC HUMAN-MOUSE SOMATIC-CELL HYBRIDS UNDER LOW AND HIGH THYMIDYLATE STRESS CONDITIONS | 1 | 3 |
| 577 | 6 | 24 | 577 1988 CYTOGENETICS AND CELL GENETICS 48(3):142-147 FANTES J; GOSDEN J; PIPER J USE OF AN ALPHOID SATELLITE SEQUENCE TO LOCATE THE X-CHROMOSOME AUTOMATICALLY, WITH PARTICULAR REFERENCE TO IDENTIFICATION OF THE FRAGILE-X | 0 | 4 |
| 578 | 20 | 37 | 578 1988 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 30(2):257-261 HO HZ; GLAHN TJ; HO JC THE FRAGILE-X SYNDROME | 2 | 3 |
| 579 | 2 | 13 | 579 1988 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 30(5):646-649 CAMMARATA S; ARCHIDIACONO N; ROMEO G; BENASSI G; GUARINO M; DALESSANDRO R PREVALENCE OF MENTAL-RETARDATION RELATED TO FRAGILE X SYNDROME AND OTHER CHROMOSOMAL-ABNORMALITIES IN THE REPUBLIC OF SAN MARINO | 0 | 2 |
| 580 | 9 | 28 | 580 1988 EPILEPSIA 29(1):41-47 MUSUMECI SA; COLOGNOLA RM; FERRI R; GIGLI GL; PETRELLA MA; SANFILIPPO S; BERGONZI P; TASSINARI CA FRAGILE-X SYNDROME - A PARTICULAR EPILEPTOGENIC EEG PATTERN | 17 | 38 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 581 | 1 | 2 | 581 1988 HUMAN GENETICS 78(2):196-197 SUBRT I; STIRSKA K FREQUENCY OF TRIRADIAL AND MULTIRADIAL CONFIGURATIONS IN FRAGILE X-CHROMOSOMES | 0 | 0 |
| 582 | 17 | 32 | 582 1988 HUMAN GENETICS 78(3):201-205 BROWN WT; GROSS A; CHAN C; JENKINS EC; MANDEL JL; OBERLE I; ARVEILER B; NOVELLI G; THIBODEAU S; HAGERMAN R; SUMMERS K; TURNER G; WHITE BN; MULLIGAN L; FORSTERGIBSON C; HOLDEN JJA; ZOLL B; KRAWCZAK M; GOONEWARDENA P; GUSTAVSON KH; PETTERSSON U; HOLMGREN G; SCHWARTZ C; HOWARDPEEBLES PN; MURPHY P; BREG WR; VEENEMA H; CARPENTER NJ MULTILOCUS ANALYSIS OF THE FRAGILE-X SYNDROME | 33 | 49 |
| 583 | 16 | 34 | 583 1988 HUMAN GENETICS 78(4):338-342 CLAYTON JF; GOSDEN CM; HASTIE ND; EVANS HJ LINKAGE HETEROGENEITY AND FRAGILE-X | 4 | 8 |
| 584 | 3 | 5 | 584 1988 HUMAN GENETICS 78(4):383-383 BUTLER MG; JOSEPH GM; RAMES LJ; CACHEIRO N; LOZZIO CB CHROMOSOME BREAKAGE IN CONTROL AND FRAGILE-X SUBJECTS USING FOLATE-DEFICIENT CULTURE CONDITIONS | 2 | 2 |
| 585 | 19 | 40 | 585 1988 HUMAN GENETICS 79(3):219-227 THIBODEAU SN; DORKINS HR; FAULK KR; BERRY R; SMITH ACM; HAGERMAN R; KING A; DAVIES KE LINKAGE ANALYSIS USING MULTIPLE DNA POLYMORPHIC MARKERS IN NORMAL-FAMILIES AND IN FAMILIES WITH FRAGILE-X SYNDROME | 13 | 23 |
| 586 | 2 | 17 | 586 1988 HUMAN GENETICS 79(3):231-234 JOHANNISSON R; FROSTERISKENIUS U; SAADALLAH N; HULTEN MA SPERMATOGENESIS IN 2 PATIENTS WITH THE FRAGILE-X SYNDROME .2. 1ST MEIOSIS - LIGHT AND ELECTRON-MICROSCOPY | 1 | 3 |
| 587 | 4 | 30 | 587 1988 HUMAN GENETICS 79(4):292-296 LI SY; TSAI CC; CHOU MY; LIN JK A CYTOGENETIC STUDY OF MENTALLY-RETARDED SCHOOL-CHILDREN IN TAIWAN WITH SPECIAL REFERENCE TO THE FRAGILE X-CHROMOSOME | 6 | 17 |
| 588 | 10 | 48 | 588 1988 HUMAN GENETICS 79(4):341-346 VANDAMME B; LIEBAERS I; HENS L; BERNHEIM JL; ROOBOL C THE ROLE OF FLUORINATED PYRIMIDINE ANALOGS IN THE INDUCTION OF THE INVITRO EXPRESSION OF THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 589 | 0 | 1 | 589 1988 HUMAN GENETICS 80(2):193-193 REKILA AM; VAISANEN ML; KAHKONEN M; LEISTI J; WINQVIST R A NEW RFLP WITH STUI AND PROBE CX55.7 (DXS105) AND ITS USEFULNESS IN CARRIER ANALYSIS OF FRAGILE X-SYNDROME | 2 | 6 |
| 590 | 16 | 24 | 590 1988 HUMAN GENETICS 80(4):375-378 VOELCKEL MA; MATTEI MG; NGUYEN C; PHILIP N; BIRG F; MATTEI JF DISSOCIATION BETWEEN MENTAL-RETARDATION AND FRAGILE SITE EXPRESSION IN A FAMILY WITH FRAGILE X-LINKED MENTAL-RETARDATION | 8 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 591 | 0 | 0 | 591 1988 JAPANESE JOURNAL OF HUMAN GENETICS 33(2):224-224 ARINAMI T; SATO M; KONDO I AUDITORY BRAIN-STEM RESPONSES IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 592 | 0 | 0 | 592 1988 JAPANESE JOURNAL OF HUMAN GENETICS 33(2):225-225 KONDO I; ARINAMI T PREVALENCE OF CHROMOSOME-ANOMALIES IN MENTALLY-RETARDED SCHOOL-CHILDREN - STUDY OF POPULATION INCIDENCE OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 593 | 0 | 0 | 593 1988 JAPANESE JOURNAL OF HUMAN GENETICS 33(2):245-245 HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M EXPRESSION OF FRA(X)(Q27.3) ASSOCIATED WITH FRAGILE-X SYNDROME | 0 | 0 |
| 594 | 6 | 30 | 594 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(1):41-52 DYKENS E; LECKMAN J; PAUL R; WATSON M COGNITIVE, BEHAVIORAL, AND ADAPTIVE FUNCTIONING IN FRAGILE-X AND NON-FRAGILE-X RETARDED MEN | 32 | 38 |
| 595 | 10 | 20 | 595 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):343-354 BREGMAN JD; LECKMAN JF; ORT SI FRAGILE X-SYNDROME - GENETIC PREDISPOSITION TO PSYCHOPATHOLOGY | 42 | 70 |
| 596 | 0 | 1 | 596 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):457-458 WOLFSCHEIN EG; JENKINS EC; SKLOWER S; COHEN IL; WISNIEWSKI KE; BROWN WT ON THE ASSOCIATION OF FRAGILE-X WITH AUTISM | 0 | 0 |
| 597 | 0 | 0 | 597 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):458-458 SCHOPLER E ON THE ASSOCIATION OF FRAGILE-X WITH AUTISM - RESPONSE | 0 | 0 |
| 598 | 2 | 6 | 598 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):458-460 LECOUTEUR A; RUTTER M; SUMMERS D; BUTLER L FRAGILE-X IN FEMALE AUTISTIC TWINS | 8 | 14 |
| 599 | 1 | 11 | 599 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(4):681-685 TSAI LY; CROWE RR; PATIL SR; MURRAY J; QUINN J SEARCH FOR DNA MARKERS IN 2 AUTISTIC MALES WITH THE FRAGILE-X SYNDROME | 2 | 3 |
| 600 | 3 | 13 | 600 1988 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 29(4):447-451 GILLBERG C; OHLSON VA; WAHLSTROM J; STEFFENBURG S; BLIX K MONOZYGOTIC FEMALE TWINS WITH AUTISM AND THE FRAGILE-X SYNDROME (AFRAX) | 9 | 19 |
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