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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 5: 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 |
|---|---|---|---|---|---|
| 401 | 6 | 19 | 401 1986 MUTATION RESEARCH 173(3):201-205 DUNCAN AMV ENHANCED SENSITIVITY OF LYMPHOBLASTOID-CELLS FROM INDIVIDUALS CARRYING THE MUTATION FOR THE FRAGILE X-SYNDROME TO THE CLASTOGENIC EFFECTS OF FUDR | 2 | 3 |
| 402 | 12 | 23 | 402 1986 NATURE 324(6093):161-163 LEDBETTER DH; LEDBETTER SA; NUSSBAUM RL IMPLICATIONS OF FRAGILE-X EXPRESSION IN NORMAL MALES FOR THE NATURE OF THE MUTATION | 31 | 56 |
| 403 | 4 | 16 | 403 1986 NEUROPSYCHOLOGIA 24(3):405-409 MIEZEJESKI CM; JENKINS EC; HILL AL; WISNIEWSKI K; FRENCH JH; BROWN WT A PROFILE OF COGNITIVE DEFICIT IN FEMALES FROM FRAGILE-X FAMILIES | 47 | 60 |
| 404 | 1 | 6 | 404 1986 NEW ENGLAND JOURNAL OF MEDICINE 315(10):607-609 TURNER G; ROBINSON H; LAING S; PURVISSMITH S PREVENTIVE SCREENING FOR THE FRAGILE-X SYNDROME | 95 | 123 |
| 405 | 0 | 0 | 405 1986 PEDIATRIC RESEARCH 20(4):A269-A269 MURPHY PD; WATSON MS; KIDD KK; BREG WR MOLECULAR APPROACHES TO CARRIER DETECTION AND PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME (MCKUSICK NUMBER 30920) | 1 | 2 |
| 406 | 0 | 0 | 406 1986 PEDIATRIC RESEARCH 20(4):A273-A273 WENGER SL; HENNESSEY JC; STEELE MW INCREASED SISTER CHROMATID EXCHANGE (SCE) AT THE FRAGILE X-SITE IN AFFECTED MALES | 0 | 0 |
| 407 | 10 | 29 | 407 1986 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 83(4):1016-1020 OBERLE I; HEILIG R; MOISAN JP; KLOEPFER C; MATTEI MG; MATTEI JF; BOUE J; FROSTERISKENIUS U; JACOBS PA; LATHROP GM; LALOUEL JM; MANDEL JL GENETIC-ANALYSIS OF THE FRAGILE-X MENTAL-RETARDATION SYNDROME WITH 2 FLANKING POLYMORPHIC DNA MARKERS | 40 | 64 |
| 408 | 0 | 0 | 408 1986 RIVISTA ITALIANA DI PEDIATRIA-ITALIAN JOURNAL OF PEDIATRICS 12(4):442-444 DELGIUDICE E; POGGI V; SARTORIO R; CARROZZO R; ROMANO A; SIRONE P; FIORE M THE FRAGILE X-SYNDROME | 0 | 0 |
| 409 | 12 | 26 | 409 1986 SOUTHERN MEDICAL JOURNAL 79(4):405-409 YOUNG RS; JARAMILLO C; MCCOMBS JL; MOORE CM; JORGENSON RJ FRAGILE-X MENTAL-RETARDATION SYNDROME TRANSMITTED THROUGH INTELLECTUALLY NORMAL MALES - IMPLICATIONS FOR GENETIC-COUNSELING | 3 | 6 |
| 410 | 24 | 48 | 410 1986 TRENDS IN NEUROSCIENCES 9(2):58-62 PEMBREY ME; WINTER RM; DAVIES KE FRAGILE X MENTAL-RETARDATION - CURRENT CONTROVERSIES | 7 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 411 | 5 | 36 | 411 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(2):184-187 HAGERMAN RJ; ALTSHULSTARK D; MCBOGG P RECURRENT OTITIS-MEDIA IN THE FRAGILE X-SYNDROME | 9 | 14 |
| 412 | 1 | 4 | 412 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(6):601-601 BARTOLUCCI G; SZATMARI P POSSIBLE SIMILARITIES BETWEEN THE FRAGILE-X AND ASPERGERS SYNDROMES | 1 | 2 |
| 413 | 1 | 1 | 413 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(6):601-602 HAGERMAN RJ POSSIBLE SIMILARITIES BETWEEN THE FRAGILE-X AND ASPERGERS SYNDROMES - REPLY | 1 | 1 |
| 414 | 8 | 19 | 414 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 26(4):909-914 WENGER SL; HENNESSEY JC; STEELE MW INCREASED SISTER CHROMATID EXCHANGE FREQUENCY AT XQ27-SITE IN AFFECTED FRAGILE-X MALES | 5 | 23 |
| 415 | 5 | 13 | 415 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 26(4):987-990 MULLEY JC; SUTHERLAND GR FRAGILE-X TRANSMISSION AND THE DETERMINATION OF CARRIER PROBABILITIES FOR GENETIC-COUNSELING | 0 | 11 |
| 416 | 12 | 29 | 416 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 27(2):401-417 LOESCH DZ; HAY DA; SUTHERLAND GR; HALLIDAY J; JUDGE C; WEBB GC PHENOTYPIC VARIATION IN MALE-TRANSMITTED FRAGILE-X - GENETIC INFERENCES | 36 | 51 |
| 417 | 7 | 20 | 417 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 27(2):435-448 MULLEY JC; GEDEON AK; THORN KA; BATES LJ; SUTHERLAND GR LINKAGE AND GENETIC-COUNSELING FOR THE FRAGILE-X USING DNA PROBE-52A, PROBE-F9, PROBE-DX13, AND PROBE-ST14 | 17 | 43 |
| 418 | 6 | 10 | 418 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 27(3):731-732 CARPENTER NJ; VEENEMA H; BAKKER E; HOFKER MH; PEARSON PL A NEW DNA PROBE PROXIMAL TO AND CLOSELY LINKED TO FRAGILE-X | 4 | 4 |
| 419 | 7 | 17 | 419 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 28(1):13-15 CHUDLEY AE; DEVONFLINDT R; HAGERMAN RJ COGNITIVE VARIABILITY IN THE FRAGILE X-SYNDROME | 5 | 9 |
| 420 | 10 | 20 | 420 1987 AMERICAN JOURNAL OF MENTAL DEFICIENCY 91(5):445-449 ROGERS RC; SIMENSEN RJ FRAGILE-X SYNDROME - A COMMON ETIOLOGY OF MENTAL-RETARDATION | 13 | 19 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 421 | 4 | 17 | 421 1987 AMERICAN JOURNAL OF MENTAL DEFICIENCY 92(2):234-236 DYKENS EM; HODAPP RM; LECKMAN JF STRENGTHS AND WEAKNESSES IN THE INTELLECTUAL-FUNCTIONING OF MALES WITH FRAGILE-X SYNDROME | 24 | 44 |
| 422 | 5 | 42 | 422 1987 AMERICAN JOURNAL ON MENTAL RETARDATION 92(3):272-278 LACHIEWICZ AM; GULLION CM; SPIRIDIGLIOZZI GA; AYLSWORTH AS DECLINING IQS OF YOUNG MALES WITH THE FRAGILE X-SYNDROME | 47 | 63 |
| 423 | 17 | 36 | 423 1987 ANNALS OF HUMAN GENETICS 51:107-124 GIANNELLI F; MORRIS AH; GARRETT C; DAKER M; THURSTON C; SMITH CAB GENETIC-HETEROGENEITY OF X-LINKED MENTAL-RETARDATION WITH FRAGILE-X - ASSOCIATION OF TIGHT LINKAGE TO FACTOR-IX AND INCOMPLETE PENETRANCE IN MALES | 7 | 16 |
| 424 | 13 | 30 | 424 1987 ARCHIVES OF OPHTHALMOLOGY 105(8):1099-1102 STORM RL; PEBENITO R; FERRETTI C OPHTHALMOLOGIC FINDINGS IN THE FRAGILE X-SYNDROME | 5 | 7 |
| 425 | 0 | 0 | 425 1987 AUSTRALIAN PAEDIATRIC JOURNAL 23(1):75-75 LOESCH DZ DERMATOGLYPHIC ABNORMALITY IN FRAGILE X-SYNDROME - A NEW CAUSAL HYPOTHESIS | 0 | 0 |
| 426 | 0 | 0 | 426 1987 AUSTRALIAN PAEDIATRIC JOURNAL 23(1):79-79 GEDEON AK; MULLEY JC; SUTHERLAND GR LINKAGE ANALYSIS AND CARRIER DETECTION OF THE FRAGILE-X | 0 | 0 |
| 427 | 0 | 0 | 427 1987 AUSTRALIAN PAEDIATRIC JOURNAL 23(1):81-81 SUTHERLAND GR; BAKER E; HOCKEY A; PURVISSMITH S THE USE OF THYMIDINE INDUCTION OF THE FRAGILE X-CHROMOSOME IN PRENATAL-DIAGNOSIS | 0 | 0 |
| 428 | 0 | 0 | 428 1987 BEHAVIOR GENETICS 17(6):642-642 VANDENBERG SG A STATUS-REPORT ON THE FRAGILE X-SYNDROME | 0 | 0 |
| 429 | 6 | 34 | 429 1987 BIOLOGICAL PSYCHIATRY 22(3):303-312 STCLAIR DM; BLACKWOOD DHR; OLIVER CJ; DICKENS P P3 ABNORMALITY IN FRAGILE-X SYNDROME | 5 | 16 |
| 430 | 2 | 4 | 430 1987 BRITISH JOURNAL OF PSYCHIATRY 150:700-702 DEB S; COWIE VA; TIMBERLAKE C A CASE OF MOSAICISM WITH FRAGILE-X AND FRAGILE-XXY COMPONENTS | 5 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 431 | 17 | 31 | 431 1987 BRITISH MEDICAL JOURNAL 295(6598):564-565 KINNELL HG FRAGILE X-SYNDROME - AN IMPORTANT PREVENTABLE CAUSE OF MENTAL HANDICAP | 2 | 2 |
| 432 | 1 | 4 | 432 1987 BRITISH MEDICAL JOURNAL 295(6603):922-922 MCKINLEY MJ; NICOLAIDES KH; KEARNEY LU; HERON O FRAGILE-X SYNDROME | 1 | 3 |
| 433 | 10 | 29 | 433 1987 CLINICAL CHEMISTRY 33(10):1726-1730 THIBODEAU SN USE OF RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM ANALYSIS FOR DETECTING CARRIERS OF FRAGILE-X SYNDROME | 1 | 1 |
| 434 | 9 | 37 | 434 1987 CLINICAL GENETICS 32(3):179-186 BORGHGRAEF M; FRYNS JP; DIELKENS A; PYCK K; VANDENBERGHE H FRAGILE (X) SYNDROME - A STUDY OF THE PSYCHOLOGICAL PROFILE IN 23 PREPUBERTAL PATIENTS | 46 | 56 |
| 435 | 0 | 0 | 435 1987 CLINICAL RESEARCH 35(1):A60-A60 EDWARDS DR; KEPPEN LD; GOLLIN SM AUTISM AND FRAGILE-X SYNDROME | 0 | 0 |
| 436 | 0 | 0 | 436 1987 CLINICAL RESEARCH 35(1):A60-A60 MIXON JC; DEV VG DIMETHYLSULFOXIDE (DMSO) INCREASES FRAGILE-X (FRA-X) EXPRESSION IN THE PRESENCE OF 5-FLOURO-2'-DEOXYURIDINE (FDUMP) | 0 | 0 |
| 437 | 0 | 0 | 437 1987 CLINICAL RESEARCH 35(1):A211-A211 HAGERMAN RJ; JACKSON AW; BERRY R; CAMPBELL J; STILLMAN E; SMITH ACM; MCGAVRAN L PREDICTORS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 438 | 1 | 22 | 438 1987 COLLEGIUM ANTROPOLOGICUM 11(2):305-316 LOESCH DZ FACTOR-ANALYSIS OF RIDGE-PATTERNS AND HAND MEASUREMENTS IN NORMAL AND FRAGILE-X MALES | 0 | 2 |
| 439 | 12 | 23 | 439 1987 CYTOGENETICS AND CELL GENETICS 44(2-3):118-122 LIN MS; SHIMANUKI K; WILSON MG EXPRESSION OF FRAGILE-X IN HUMAN-MOUSE SOMATIC-CELL HYBRIDS | 1 | 1 |
| 440 | 0 | 0 | 440 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):587-587 BROWN WT; WU Y; GROSS AC; CHAN CB; DOBKIN CS; JENKINS EC; CARPENTER N LINKAGE OF FLANKING PROBES IN 40 FRAGILE X-FAMILIES | 1 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 441 | 0 | 0 | 441 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):594-594 CLAYTON JF; GOSDEN CM; HASTIE N; EVANS HJ MULTIPOINT ANALYSIS AND FRAGILE-X | 0 | 0 |
| 442 | 0 | 0 | 442 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):598-598 CONNOR JM; OSMAN H; STEFANI L; NEVIN NC; HOFKER M LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE-X SYNDROME USING CX55-7 (DXS105) | 0 | 2 |
| 443 | 0 | 0 | 443 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):622-622 GOSDEN C; BUCHANAN J; NEWTON M; KESTON M; WRIGHT AF; PRIMROSE D; CLAYTON JF; CHRISTIE S; HASTIE N; EVANS HJ FRAGILE-X SYNDROME - NEW LINKAGE DATA IN 10 FAMILIES | 0 | 0 |
| 444 | 0 | 0 | 444 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):688-689 SCHWARTZ C; PATTERSON M; DAVIES K; TRUNCA C; TRASK B; PHELAN MC THE USE OF DISTAL DELETIONS OF XQ TO ORDER LOCI BETWEEN FACTOR-IX AND THE FRAGILE-X SITE (XQ27.3) | 1 | 2 |
| 445 | 0 | 0 | 445 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):690-690 SENIOR J; KILPATRICK M; WEBB T LINKAGE STUDIES IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 446 | 9 | 27 | 446 1987 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 29(6):711-719 THAKE A; TODD J; WEBB T; BUNDEY S CHILDREN WITH THE FRAGILE X-CHROMOSOME AT SCHOOLS FOR THE MILDLY MENTALLY-RETARDED | 11 | 15 |
| 447 | 15 | 42 | 447 1987 GENETICS 117(3):587-599 LAIRD CD PROPOSED MECHANISM OF INHERITANCE AND EXPRESSION OF THE HUMAN FRAGILE-X SYNDROME OF MENTAL-RETARDATION | 92 | 167 |
| 448 | 6 | 9 | 448 1987 GENETIKA 23(3):504-509 SULEIMANOVA DG; KULESHOV NP SPONTANEOUS AND INDUCED CHROMOSOMAL INSTABILITY IN PATIENTS WITH FRAGILE X-CHROMOSOME, SUFFERING FROM X-LINKED MENTAL-RETARDATION | 1 | 3 |
| 449 | 1 | 2 | 449 1987 HASTINGS CENTER REPORT 17(1):2-3 [Anon] TO SCREEN OR NOT TO SCREEN FOR THE FRAGILE X-SYNDROME | 0 | 0 |
| 450 | 0 | 15 | 450 1987 HUMAN GENETICS 75(1):4-6 AMAROSE AP; HUTTENLOCHER PR; SPRUDZS RM; LAITSCH TJ; PETTENATI MJ A HERITABLE FRAGILE 12Q24.13 SEGREGATING IN A FAMILY WITH THE FRAGILE X-CHROMOSOME | 2 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 451 | 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 |
| 452 | 8 | 14 | 452 1987 HUMAN GENETICS 75(3):294-295 BROWN WT; SHERMAN SL; DOBKIN CS HYPOTHESIS REGARDING THE NATURE OF THE FRAGILE-X MUTATION - A REPLY | 3 | 5 |
| 453 | 23 | 47 | 453 1987 HUMAN GENETICS 75(4):311-321 BROWN WT; JENKINS EC; GROSS AC; CHAN CB; KRAWCZUN MS; DUNCAN CJ; SKLOWER SL; FISCH GS FURTHER EVIDENCE FOR GENETIC-HETEROGENEITY IN THE FRAGILE-X SYNDROME | 33 | 53 |
| 454 | 7 | 33 | 454 1987 HUMAN GENETICS 76(2):141-147 JOHANNISSON R; REHDER H; WENDT V; SCHWINGER E SPERMATOGENESIS IN 2 PATIENTS WITH THE FRAGILE-X SYNDROME .1. HISTOLOGY - LIGHT AND ELECTRON-MICROSCOPY | 8 | 15 |
| 455 | 16 | 30 | 455 1987 HUMAN GENETICS 76(2):165-172 BUCHANAN JA; BUCKTON KE; GOSDEN CM; NEWTON MS; CLAYTON JF; CHRISTIE S; HASTIE N 10 FAMILIES WITH FRAGILE-X SYNDROME - LINKAGE RELATIONSHIPS WITH 4 DNA PROBES FROM DISTAL-XQ | 9 | 16 |
| 456 | 14 | 26 | 456 1987 HUMAN GENETICS 76(4):344-347 ARINAMI T; KONDO I; NAKAJIMA S; HAMAGUCHI H FREQUENCY OF THE FRAGILE X-SYNDROME IN INSTITUTIONALIZED MENTALLY-RETARDED FEMALES IN JAPAN | 7 | 9 |
| 457 | 8 | 27 | 457 1987 HUMAN GENETICS 77(1):60-65 OBERLE I; CAMERINO G; WROGEMANN K; ARVEILER B; HANAUER A; RAIMONDI E; MANDEL JL MULTIPOINT GENETIC-MAPPING OF THE XQ26-Q28 REGION IN FAMILIES WITH FRAGILE-X MENTAL-RETARDATION AND IN NORMAL-FAMILIES REVEALS TIGHT LINKAGE OF MARKERS IN Q26-Q27 | 17 | 60 |
| 458 | 7 | 20 | 458 1987 HUMAN GENETICS 77(1):85-87 KAHKONEN M; ALITALO T; AIRAKSINEN E; MATILAINEN R; LAUNIALA K; AUTIO S; LEISTI J PREVALENCE OF THE FRAGILE-X SYNDROME IN 4 BIRTH COHORTS OF CHILDREN OF SCHOOL AGE | 31 | 45 |
| 459 | 4 | 11 | 459 1987 HUMAN GENETICS 77(1):92-94 ARINAMI T; KONDO I; HAMAGUCHI H; TAMURA K; HIRANO T A FRAGILE-X FEMALE WITH DOWN-SYNDROME | 8 | 11 |
| 460 | 10 | 12 | 460 1987 HUMAN GENETICS 77(3):297-298 WINTER R; PEMBREY M INTERPRETATION OF THE HETEROGENEITY IN THE LINKAGE RELATIONSHIPS OF DNA MARKERS AROUND THE FRAGILE-X LOCUS | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 461 | 0 | 0 | 461 1987 INTERNATIONAL JOURNAL OF NEUROSCIENCE 34(3-4):172-172 FERRI R; BERGONZI P; COLOGNOLA RM; MUSUMECI SA; PETRELLA MA; SANFILIPPO S; VIGLIANESI A; GIGLI GL BRAIN-STEM AUDITORY AND VISUAL EVOKED-POTENTIALS IN FRAGILE-X MENTAL-RETARDATION SYNDROME SUBJECTS | 0 | 0 |
| 462 | 0 | 0 | 462 1987 JAPANESE JOURNAL OF GENETICS 62(6):520-520 HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M STRUCTURAL ALTERATION IN FRA(X)(Q27.3) ASSOCIATED WITH FRAGILE-X SYNDROME | 0 | 0 |
| 463 | 0 | 0 | 463 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):122-123 SUGIO Y FRAGILE-X SYNDROME - COLLABORATIVE STUDIES OF JAPANESE PATIENTS | 0 | 0 |
| 464 | 0 | 0 | 464 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):170-171 ARINAMI T; NAKAJIMA S; KONDO I THE FRAGILE X-SYNDROME IN A JAPANESE POPULATION OF INSTITUTIONALIZED MENTALLY-RETARDED FEMALES | 0 | 0 |
| 465 | 0 | 0 | 465 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):171-171 KASAI R; NARAHARA K; MURAKAMI M; KIKKAWA K; KIMURA S; HIRAMOTO K; KIMOTO H PREVALENCE OF THE FRAGILE(X) SYNDROME IN INSTITUTIONALIZED MENTALLY-RETARDED INDIVIDUALS | 0 | 0 |
| 466 | 0 | 0 | 466 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):210-211 ARINAMI T; TAMURA K; KONDO I A FRAGILE X-FEMALE WITH DOWN-SYNDROME - A CASE-REPORT | 0 | 0 |
| 467 | 11 | 41 | 467 1987 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 17(4):457-468 PAUL R; DYKENS E; LECKMAN JF; WATSON M; BREG WR; COHEN DJ A COMPARISON OF LANGUAGE CHARACTERISTICS OF MENTALLY-RETARDED ADULTS WITH FRAGILE-X SYNDROME AND THOSE WITH NONSPECIFIC MENTAL-RETARDATION AND AUTISM | 19 | 26 |
| 468 | 16 | 41 | 468 1987 JOURNAL OF MEDICAL GENETICS 24(1):14-22 CONNOR JM; PIRRIT LA; YATES JRW; CROSSLEY JA; IMRIE SJ; COLGAN JM LINKAGE ANALYSIS USING MULTIPLE XQ DNA POLYMORPHISMS IN NORMAL-FAMILIES, FAMILIES WITH THE FRAGILE X-SYNDROME, AND OTHER FAMILIES WITH X-LINKED CONDITIONS | 7 | 12 |
| 469 | 17 | 38 | 469 1987 JOURNAL OF MEDICAL GENETICS 24(1):23-31 VEENEMA H; GERAEDTS JPM; BEVERSTOCK GC; PEARSON PL THE FRAGILE X-SYNDROME IN A LARGE FAMILY .1. CYTOGENETIC AND CLINICAL INVESTIGATIONS | 14 | 21 |
| 470 | 5 | 21 | 470 1987 JOURNAL OF MEDICAL GENETICS 24(1):32-38 VEENEMA H; VEENEMA T; GERAEDTS JPM THE FRAGILE X-SYNDROME IN A LARGE FAMILY .2. PSYCHOLOGICAL INVESTIGATIONS | 28 | 39 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 471 | 0 | 0 | 471 1987 JOURNAL OF MEDICAL GENETICS 24(4):240-240 WINTER RM POPULATION-GENETICS IMPLICATIONS OF THE PREMUTATION HYPOTHESIS FOR THE GENERATION OF THE FRAGILE-X MENTAL-RETARDATION GENE | 0 | 0 |
| 472 | 13 | 33 | 472 1987 JOURNAL OF MEDICAL GENETICS 24(7):413-421 VEENEMA H; CARPENTER NJ; BAKKER E; HOFKER MH; WARD AM; PEARSON PL THE FRAGILE-X SYNDROME IN A LARGE FAMILY .3. INVESTIGATIONS ON LINKAGE OF FLANKING DNA MARKERS WITH THE FRAGILE SITE-XQ27 | 17 | 38 |
| 473 | 0 | 0 | 473 1987 JOURNAL OF MEDICAL GENETICS 24(10):635-635 CONNOR JM; OSMAN H; STEPHANIE L; NEVIN NC; HOFKER M LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE X SYNDROME USING CX55-7 (DXS105) | 3 | 3 |
| 474 | 0 | 0 | 474 1987 JOURNAL OF MEDICAL GENETICS 24(10):640-640 SENIOR J; KILPATRICK M; WEBB T COMPARATIVE LINKAGE STUDIES IN THE FRAGILE X-SYNDROME | 1 | 1 |
| 475 | 0 | 0 | 475 1987 JOURNAL OF MEDICAL GENETICS 24(10):641-641 HULTEN M; JOHANNISSON R MEIOSIS IN THE FRAGILE-X MENTAL-RETARDATION SYNDROME | 1 | 1 |
| 476 | 4 | 18 | 476 1987 JOURNAL OF MENTAL DEFICIENCY RESEARCH 31:73-79 PUESCHEL SM; OBRIEN MM; PADREMENDOZA T KLINEFELTER SYNDROME AND ASSOCIATED FRAGILE-X SYNDROME | 7 | 8 |
| 477 | 2 | 4 | 477 1987 JOURNAL OF MENTAL DEFICIENCY RESEARCH 31:81-85 COWIE VA; SINGH KR; WHEATER R; BIRD J THE FRAGILE-X SYNDROME IN TWIN SISTERS | 1 | 1 |
| 478 | 32 | 85 | 478 1987 JOURNAL OF PEDIATRICS 110(6):821-831 CHUDLEY AE; HAGERMAN RJ FRAGILE-X SYNDROME | 53 | 80 |
| 479 | 56 | 112 | 479 1987 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 26(4):463-471 BREGMAN JD; DYKENS E; WATSON M; ORT SI; LECKMAN JF FRAGILE-X SYNDROME - VARIABILITY OF PHENOTYPIC-EXPRESSION | 23 | 40 |
| 480 | 11 | 25 | 480 1987 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 26(4):589-592 GOLDFINE PE; MCPHERSON PM; HARDESTY VA; HEATH GA; BEAUREGARD LJ; BAKER AA FRAGILE-X CHROMOSOME ASSOCIATED WITH PRIMARY LEARNING-DISABILITY | 12 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 481 | 4 | 5 | 481 1987 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 26(6):938-938 HAGERMAN RJ FRAGILE-X CHROMOSOME AND LEARNING-DISABILITY | 0 | 0 |
| 482 | 6 | 10 | 482 1987 LANCET 1(8527):280-280 BROWN WT; WU Y; GROSS AC; CHAN CB; DOBKIN CS; JENKINS EC RFLP FOR LINKAGE ANALYSIS OF FRAGILE-X SYNDROME | 21 | 35 |
| 483 | 1 | 2 | 483 1987 LANCET 2(8554):329-329 VERLOES A; SACRE JP; GEUBELLE F SOTOS SYNDROME AND FRAGILE-X CHROMOSOMES | 1 | 5 |
| 484 | 3 | 36 | 484 1987 NEUROPSYCHOLOGIA 25(6):881-891 GRIGSBY JP; KEMPER MB; HAGERMAN RJ DEVELOPMENTAL GERSTMANN SYNDROME WITHOUT APHASIA IN FRAGILE-X SYNDROME | 16 | 27 |
| 485 | 4 | 4 | 485 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 BURD L THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 486 | 0 | 1 | 486 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 TURNER G THE FRAGILE X-CHROMOSOME - REPLY | 1 | 1 |
| 487 | 0 | 0 | 487 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 HECHT F; HECHT BK THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 488 | 0 | 0 | 488 1987 PEDIATRIC NEUROLOGY 3(5):284-287 MATSUISHI T; SHIOTSUKI Y; NIIKAWA N; KATAFUCHI Y; OTAKI E; ANDO H; YAMASHITA Y; HORIKAWA M; URABE F; KURIYA N; YAMASHITA F FRAGILE-X SYNDROME IN JAPANESE PATIENTS WITH INFANTILE-AUTISM | 4 | 6 |
| 489 | 0 | 0 | 489 1987 PEDIATRIC RESEARCH 21(4):A230-A230 SHAPIRO LR; WILMOT PL; OMAR RA; DAVIDIAN MM; CHANDER PN PRENATAL PATHOGENESIS OF MACROORCHIDISM IN THE FRAGILE X-SYNDROME | 0 | 0 |
| 490 | 0 | 0 | 490 1987 PRACTITIONER 231(1431):910-& BUNDEY S THE FRAGILE X-SYNDROME | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 491 | 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 |
| 492 | 12 | 22 | 492 1987 PRENATAL DIAGNOSIS 7(3):203-214 WEBB TP; RODECK CH; NICOLAIDES KH; GOSDEN CM PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME USING FETAL BLOOD AND AMNIOTIC-FLUID | 9 | 18 |
| 493 | 12 | 37 | 493 1987 SCIENCE 237(4813):420-423 WARREN ST; ZHANG FP; LICAMELI GR; PETERS JF THE FRAGILE-X SITE IN SOMATIC-CELL HYBRIDS - AN APPROACH FOR MOLECULAR-CLONING OF FRAGILE SITES | 29 | 71 |
| 494 | 0 | 0 | 494 1987 TERATOLOGY 36(3):453-453 SUZUKI Y; CHYO H; MATSUI A; SHIMOMURA C; FUNAHASI M CLINICAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 1 | 2 |
| 495 | 17 | 44 | 495 1988 AMERICAN JOURNAL OF DISEASES OF CHILDREN 142(11):1216-1221 HAGERMAN R; BERRY R; JACKSON AW; CAMPBELL J; SMITH ACM; MCGAVRAN L INSTITUTIONAL SCREENING FOR THE FRAGILE-X SYNDROME | 12 | 21 |
| 496 | 12 | 30 | 496 1988 AMERICAN JOURNAL OF HUMAN GENETICS 42(2):380-389 ARVEILER B; OBERLE I; VINCENT A; HOFKER MH; PEARSON PL; MANDEL JL GENETIC-MAPPING OF THE XQ27-Q28 REGION - NEW RFLP MARKERS USEFUL FOR DIAGNOSTIC APPLICATIONS IN FRAGILE-X AND HEMOPHILIA-B FAMILIES | 22 | 61 |
| 497 | 10 | 24 | 497 1988 AMERICAN JOURNAL OF HUMAN GENETICS 43(1):46-51 ARINAMI T; SATO M; NAKAJIMA S; KONDO I AUDITORY BRAIN-STEM RESPONSES IN THE FRAGILE-X SYNDROME | 8 | 11 |
| 498 | 8 | 31 | 498 1988 AMERICAN JOURNAL OF HUMAN GENETICS 43(5):684-688 PATTERSON M; BELL M; KRESS W; DAVIES KE; FROSTERISKENIUS U LINKAGE STUDIES IN A LARGE FRAGILE X-FAMILY | 10 | 23 |
| 499 | 1 | 3 | 499 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):1-17 NERI G; OPITZ JM; MIKKELSEN M; JACOBS PA; DAVIES K; TURNER G CONFERENCE REPORT - 3RD INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 6 | 15 |
| 500 | 0 | 0 | 500 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):20-20 KAHKONEN M; ALITALO T; AIRAKSINEN E; MATILAINER R; LAUNIALA K; AUTIO S; LEISTI J PREVALENCE OF THE FRAGILE-X OR MARTIN-BELL SYNDROME | 0 | 0 |
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