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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by journal name.
Page 15: 1 (A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT) 2 (AMERICAN JOURNAL OF HUMAN GENETICS) 3 (AMERICAN JOURNAL OF HUMAN GENETICS) 4 (AMERICAN JOURNAL OF HUMAN GENETICS) 5 (AMERICAN JOURNAL OF MEDICAL GENETICS) 6 (AMERICAN JOURNAL OF MEDICAL GENETICS) 7 (AMERICAN JOURNAL OF MEDICAL GENETICS) 8 (AMERICAN JOURNAL OF MEDICAL GENETICS) 9 (AMERICAN JOURNAL OF MEDICAL GENETICS) 10 (ANNALS OF NEUROLOGY) 11 (BIOPHYSICAL JOURNAL) 12 (CLINICAL GENETICS) 13 (CURRENT BIOLOGY) 14 (DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY) 15 (GENETIC TESTING) 16 (HUMAN GENETICS) 17 (JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION) 18 (JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS) 19 (JOURNAL OF MEDICAL GENETICS) 20 (JOURNAL OF NEUROSCIENCE RESEARCH) 21 (MEDICAL ANTHROPOLOGY QUARTERLY) 22 (NATURE REVIEWS NEUROSCIENCE) 23 (PEDIATRIC RESEARCH) 24 (REVISTA DE NEUROLOGIA)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1401 | 4 | 6 | 2018 2001 GENETIC TESTING 5(2):139-140 Gilbert F Comment: How many are too many when discussing triplet repeats in the FMR1 gene and the fragile X syndrome? | 0 | 1 |
| 1402 | 26 | 34 | 2265 2003 GENETIC TESTING 7(4):303-308 Gasteiger M; Grasbon-Frod E; Neitzel B; Kooy F; Holinski-Feder E FMR1 gene deletion/reversion: A pitfall of fragile X carrier testing | 0 | 0 |
| 1403 | 19 | 29 | 2266 2003 GENETIC TESTING 7(4):339-343 Rife M; Badenas C; Mallolas J; Jimenez L; Cervera R; Maya A; Glover G; Rivera F; Mila M Incidence of Fragile X in 5,000 consecutive newborn males | 0 | 0 |
| 1404 | 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 |
| 1405 | 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 |
| 1406 | 1 | 42 | 2019 2001 GENETICS 157(2):717-725 Su MA; Wisotzkey RG; Newfeld SJ A screen for modifiers of decapentaplegic mutant phenotypes identifies lilliputian, the only member of the Fragile-X/Burkitt's lymphoma family of transcription factors in Drosophila melanogaster | 0 | 6 |
| 1407 | 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 |
| 1408 | 5 | 14 | 1788 1999 GENETICS AND MOLECULAR BIOLOGY 22(4):471-474 Vianna-Morgante AM; Costa SS; Pavanello RDM; Otto PA; Mingroni-Netto RC Premature ovarian failure (POF) in Brazilian fragile X carriers | 1 | 4 |
| 1409 | 29 | 49 | 2142 2002 GENETICS AND MOLECULAR BIOLOGY 25(1):1-6 de Diego Y; Hmadcha A; Moron F; Lucas M; Carrasco M; Pintado E Fragile X founder effect and distribution of CGG repeats among the mentally retarded population of Andalusia, South Spain | 0 | 0 |
| 1410 | 27 | 44 | 1891 2000 GENETICS IN MEDICINE 2(4):242-248 Burman RW; Anoe KS; Popovich BW Fragile X full mutations ave more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1411 | 99 | 154 | 2020 2001 GENETICS IN MEDICINE 3(5):359-371 Crawford DC; Acuna JM; Sherman SL FMR1 and the fragile X syndrome: Human genome epidemiology review | 13 | 20 |
| 1412 | 15 | 55 | 2268 2003 GENETICS IN MEDICINE 5(5):378-384 Skinner D; Sparkman KL; Bailey DB Screening for fragile X syndrome: Parent attitudes and perspectives | 1 | 1 |
| 1413 | 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 |
| 1414 | 13 | 23 | 1091 1993 GENETIKA 29(6):1026-1034 BARANOV VS; ASEEV MV; RAKISHEVA ZB; KULESHOV NP; MARINICHEVA GS; BYCHKOVA AM; ZUKIN VD; LEDASCHEVA EA; AMOASHYI DS; KUZNETZOVA TV; VAHARLOVSKY VG MOLECULAR DIAGNOSIS OF FRAGILE X-SYNDROME (SYN MARTIN-BELL) IN THE PATIENTS OF NATIVE POPULATIONS | 0 | 2 |
| 1415 | 5 | 48 | 2021 2001 GENOME RESEARCH 11(8):1382-1391 Mathews DJ; Kashuk C; Brightwell G; Eichler EE; Chakravarti A Sequence variation within the fragile x locus | 0 | 3 |
| 1416 | 0 | 0 | 639 1989 GENOMICS 4(4):570-578 PATTERSON MN; BELL MV; BLOOMFIELD J; FLINT T; DORKINS H; THIBODEAU SN; SCHAID D; BREN G; SCHWARTZ CE; WIERINGA B; ROPERS HH; CALLEN DF; SUTHERLAND G; FROSTERISKENIUS U; VISSING H; DAVIES KE GENETIC AND PHYSICAL MAPPING OF A NOVEL REGION CLOSE TO THE FRAGILE X-SITE ON THE HUMAN X-CHROMOSOME | 17 | 43 |
| 1417 | 0 | 0 | 640 1989 GENOMICS 5(4):797-801 VINCENT A; DAHL N; OBERLE I; HANAUER A; MANDEL JL; MALMGREN H; PETTERSSON U THE POLYMORPHIC MARKER DXS304 IS WITHIN 5-CENTIMORGANS OF THE FRAGILE-X LOCUS | 13 | 23 |
| 1418 | 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 |
| 1419 | 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 |
| 1420 | 6 | 24 | 978 1992 GENOMICS 12(4):814-817 FAUST CJ; VERKERK AJMH; WILSON PJ; MORRIS CP; HOPWOOD JJ; OOSTRA BA; HERMAN GE GENETIC-MAPPING ON THE MOUSE X-CHROMOSOME OF HUMAN CDNA CLONES FOR THE FRAGILE-X AND HUNTER SYNDROMES | 0 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1421 | 6 | 25 | 979 1992 GENOMICS 12(4):818-821 LAVAL SH; BLAIR HJ; HIRST MC; DAVIES KE; BOYD Y MAPPING OF FMR1, THE GENE IMPLICATED IN FRAGILE X-LINKED MENTAL-RETARDATION, ON THE MOUSE X-CHROMOSOME | 0 | 9 |
| 1422 | 40 | 62 | 1480 1996 GIORNALE DI NEUROPSICHIATRIA DELL ETA EVOLUTIVA 16(2):147-154 Veneselli E; Biancheri R; Perrone MV Neuropsychiatric aspects in the fragile X syndrome | 0 | 0 |
| 1423 | 31 | 55 | 2330 2004 GROWTH HORMONE & IGF RESEARCH 14:S158-S165 Mandel JL; Biancalana V Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues | 0 | 0 |
| 1424 | 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 |
| 1425 | 14 | 32 | 280 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 |
| 1426 | 5 | 10 | 1789 1999 HEREDITAS 130(2):189-190 Sucharov CC; Silva R; Rondinelli E; Moura-Neto RS Fragile X trinucleotide repeats from a normal population in Rio de Janeiro, Brazil | 0 | 0 |
| 1427 | 1 | 5 | 58 1982 HOSPITAL PRACTICE 17(7):17-& BROWN WT; JENKINS EC FRAGILE X - ITS DETECTABILITY | 1 | 1 |
| 1428 | 5 | 8 | 1588 1997 HOSPITAL PRACTICE 32(4):73-& Warren ST Trinucleotide repetition and fragile X syndrome | 3 | 5 |
| 1429 | 15 | 44 | 2143 2002 HUMAN BRAIN MAPPING 16(4):206-218 Rivera SM; Menon V; White CD; Glaser B; Reiss AL Functional brain activation during arithmetic processing in females with fragile X Syndrome is related to FMRI protein expression | 7 | 13 |
| 1430 | 1 | 17 | 18 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1431 | 0 | 3 | 19 1981 HUMAN GENETICS 59(2):186-186 FONATSCH C A SIMPLE METHOD TO DEMONSTRATE THE FRAGILE X-CHROMOSOME IN FIBROBLASTS | 21 | 38 |
| 1432 | 2 | 40 | 20 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 |
| 1433 | 0 | 5 | 59 1982 HUMAN GENETICS 60(1):80-81 ZANKL H; EBERLE G METHODS OF INCREASING THE VISIBILITY OF FRAGILE-X CHROMOSOMES | 5 | 8 |
| 1434 | 4 | 23 | 60 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 |
| 1435 | 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 |
| 1436 | 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 |
| 1437 | 2 | 5 | 63 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 |
| 1438 | 2 | 3 | 64 1982 HUMAN GENETICS 61(3):262-263 FRYNS JP; VANDENBERGHE H TRANSMISSION OF FRAGILE (X)(Q27) FROM NORMAL MALE(S) | 25 | 35 |
| 1439 | 1 | 12 | 65 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 | 21 | 30 |
| 1440 | 5 | 13 | 66 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1441 | 8 | 23 | 134 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 |
| 1442 | 5 | 17 | 135 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 |
| 1443 | 6 | 26 | 136 1983 HUMAN GENETICS 64(3):240-245 NIELSEN KB; TOMMERUP N; POULSEN H; JACOBSEN P; BECK B; MIKKELSEN M 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 |
| 1444 | 3 | 9 | 137 1983 HUMAN GENETICS 65(1):88-89 SOUDEK D; EMANUEL M A FRAGILE X SUPPRESSOR IN THE NORMAL HUMAN-BLOOD | 3 | 4 |
| 1445 | 0 | 9 | 201 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 |
| 1446 | 0 | 1 | 202 1984 HUMAN GENETICS 66(1):100-100 GARDNER RJM FRAGILE-X HOMOZYGOSITY DUE TO SOMATIC CROSSING-OVER | 1 | 2 |
| 1447 | 3 | 24 | 203 1984 HUMAN GENETICS 67(1):99-102 CANTU ES; JACOBS PA FRAGILE (X) EXPRESSION - RELATIONSHIP TO THE CELL-CYCLE | 4 | 7 |
| 1448 | 2 | 10 | 204 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 |
| 1449 | 3 | 6 | 205 1984 HUMAN GENETICS 68(4):346-347 DEARCE MA VERIFICATION OF LYONS HYPOTHESIS IN FRAGILE-X CARRIERS | 2 | 5 |
| 1450 | 1 | 15 | 281 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1451 | 1 | 9 | 282 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 |
| 1452 | 5 | 19 | 283 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 | 19 | 33 |
| 1453 | 13 | 28 | 284 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 |
| 1454 | 11 | 40 | 285 1985 HUMAN GENETICS 69(4):289-299 SHERMAN SL; JACOBS PA; MORTON NE; FROSTERISKENIUS U; HOWARDPEEBLES PN; NIELSEN KB; PARTINGTON MW; SUTHERLAND GR; TURNER G; WATSON M FURTHER SEGREGATION ANALYSIS OF THE FRAGILE-X SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES | 226 | 348 |
| 1455 | 2 | 17 | 286 1985 HUMAN GENETICS 69(4):327-331 MATTEI MG; BAETEMAN MA; HEILIG R; OBERLE I; DAVIES K; MANDEL JL; MATTEI JF 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 |
| 1456 | 17 | 40 | 287 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 |
| 1457 | 3 | 5 | 288 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 |
| 1458 | 2 | 3 | 289 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 |
| 1459 | 3 | 15 | 385 1986 HUMAN GENETICS 73(1):20-22 ABRUZZO MA; PETTAY D; MAYER M; JACOBS PA THE EFFECT OF CAFFEINE ON FRAGILE-X EXPRESSION | 9 | 12 |
| 1460 | 4 | 14 | 386 1986 HUMAN GENETICS 73(4):309-312 ARINAMI T; KONDO I; NAKAJIMA S FREQUENCY OF THE FRAGILE X-SYNDROME IN JAPANESE MENTALLY-RETARDED MALES | 23 | 29 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1461 | 9 | 16 | 387 1986 HUMAN GENETICS 74(1):93-97 WINTER RM; PEMBREY ME ANALYSIS OF LINKAGE RELATIONSHIPS BETWEEN GENETIC-MARKERS AROUND THE FRAGILE X LOCUS WITH SPECIAL REFERENCE TO THE DAUGHTERS OF NORMAL TRANSMITTING MALES | 13 | 17 |
| 1462 | 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 |
| 1463 | 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 |
| 1464 | 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 |
| 1465 | 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 |
| 1466 | 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 |
| 1467 | 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 |
| 1468 | 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 |
| 1469 | 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 |
| 1470 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1471 | 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 |
| 1472 | 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 |
| 1473 | 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 |
| 1474 | 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 |
| 1475 | 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 |
| 1476 | 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 |
| 1477 | 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 |
| 1478 | 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 |
| 1479 | 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 |
| 1480 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1481 | 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 |
| 1482 | 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 |
| 1483 | 4 | 22 | 641 1989 HUMAN GENETICS 81(4):377-381 TOMMERUP N INDUCTION OF THE FRAGILE X ON BRDU-SUBSTITUTED CHROMOSOMES WITH DIRECT VISUALIZATION OF SISTER CHROMATID EXCHANGES ON BANDED CHROMOSOMES | 4 | 4 |
| 1484 | 10 | 17 | 642 1989 HUMAN GENETICS 82(1):79-81 SCHAAP T THE ROLE OF RECOMBINATION IN THE EVOLVEMENT OF THE FRAGILE X-MUTATION | 2 | 2 |
| 1485 | 7 | 16 | 643 1989 HUMAN GENETICS 82(3):216-218 DAHL N; HAMMARSTROMHEEROMA K; GOONEWARDENA P; WADELIUS C; GUSTAVSON KH; HOLMGREN G; VANOMMEN GJB; PETTERSSON U ISOLATION OF A DNA PROBE OF POTENTIAL USE FOR DIAGNOSIS OF THE FRAGILE-X SYNDROME | 17 | 32 |
| 1486 | 6 | 12 | 700 1990 HUMAN GENETICS 84(2):216-217 BUTLER MG NO SIGNIFICANT RELATIONSHIP BETWEEN AGE AND FREQUENCY OF CHROMOSOME LESIONS IN MENTALLY-RETARDED INDIVIDUALS WITH OR WITHOUT THE FRAGILE X-SYNDROME | 1 | 4 |
| 1487 | 5 | 14 | 701 1990 HUMAN GENETICS 84(3):263-266 ROUSSEAU F; VINCENT A; OBERLE I; MANDEL JL NEW INFORMATIVE POLYMORPHISM AT THE DXS304 LOCUS, A CLOSE DISTAL MARKER FOR THE FRAGILE X-LOCUS | 4 | 19 |
| 1488 | 6 | 44 | 702 1990 HUMAN GENETICS 84(4):347-352 SCHMIDT M; CERTOMA A; DUSART D; KALITSIS P; LEVERSHA M; FOWLER K; SHEFFIELD L; JACK I; DANKS DM UNUSUAL X-CHROMOSOME INACTIVATION IN A MENTALLY-RETARDED GIRL WITH AN INTERSTITIAL DELETION XQ27 - IMPLICATIONS FOR THE FRAGILE X-SYNDROME | 7 | 27 |
| 1489 | 5 | 7 | 703 1990 HUMAN GENETICS 85(1):141-142 SUTHERS GK; SUTHERLAND GR RECOMBINATION AND THE FRAGILE-X | 0 | 0 |
| 1490 | 8 | 33 | 704 1990 HUMAN GENETICS 85(3):267-271 LI SY; LIN JK DIFFERENTIAL BLEOMYCIN SUSCEPTIBILITY IN CULTURED LYMPHOCYTES OF FRAGILE X-PATIENTS AND NORMAL INDIVIDUALS | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1491 | 9 | 21 | 705 1990 HUMAN GENETICS 85(6):590-594 YU WD; WENGER SL; STEELE MW X-CHROMOSOME IMPRINTING IN FRAGILE-X SYNDROME | 6 | 15 |
| 1492 | 24 | 65 | 706 1990 HUMAN GENETICS 85(6):659-665 WOHRLE D; FRYNS JP; STEINBACH P FRAGILE-X EXPRESSION AND FRAGILE-X INACTIVATION .1. THE EXPRESSION OF THE FRAGILE SITE AT XQ27.3 IS NOT SUPPRESSED ON INACTIVE X-CHROMOSOMES SEPARATED FROM THE ACTIVE HOMOLOG | 7 | 9 |
| 1493 | 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 |
| 1494 | 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 |
| 1495 | 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 |
| 1496 | 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 |
| 1497 | 37 | 55 | 980 1992 HUMAN GENETICS 88(3):335-343 FOLLETTE PJ; LAIRD CD ESTIMATING THE STABILITY OF THE PROPOSED IMPRINTED STATE OF THE FRAGILE-X MUTATION WHEN TRANSMITTED BY FEMALES | 2 | 3 |
| 1498 | 13 | 18 | 981 1992 HUMAN GENETICS 89(1):114-116 WOHRLE D; HIRST MC; KENNERKNECHT I; DAVIES KE; STEINBACH P GENOTYPE MOSAICISM IN FRAGILE-X FETAL TISSUES | 32 | 43 |
| 1499 | 20 | 36 | 982 1992 HUMAN GENETICS 90(1-2):55-61 ERSTER SH; BROWN WT; GOONEWARDENA P; DOBKIN CS; JENKINS EC; PERGOLIZZI RG POLYMERASE CHAIN-REACTION ANALYSIS OF FRAGILE X-MUTATIONS | 18 | 30 |
| 1500 | 8 | 14 | 1092 1993 HUMAN GENETICS 91(1):80-82 DREESEN JCFM; VANDENHURK JAJM; SMITS APT; VANDENOUWELAND AMW; MARKSLAG PWB; VANOOST BA DXS539, A POLYMORPHIC DNA MARKER PROXIMAL OF THE FRAGILE-X GENE | 0 | 2 |
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