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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 |
|---|---|---|---|---|---|
| 1501 | 2 | 6 | 155 1983 NEW ENGLAND JOURNAL OF MEDICINE 308(23):1424-1424 HAGERMAN RJ; LEVITAS A DILANTIN AND THE FRAGILE X-SYNDROME | 0 | 2 |
| 1502 | 1 | 6 | 190 1984 CHINESE MEDICAL JOURNAL 97(11):861-864 XU BZ; REN S; XIAO GF; ZHOU XT A FRAGILE X SYNDROME FAMILY | 0 | 1 |
| 1503 | 3 | 6 | 205 1984 HUMAN GENETICS 68(4):346-347 DEARCE MA VERIFICATION OF LYONS HYPOTHESIS IN FRAGILE-X CARRIERS | 2 | 5 |
| 1504 | 2 | 6 | 211 1984 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 14(4):451-452 JACKSON A; HOGERMAN R; LEVITAS A SEROTONIN LEVELS IN FRAGILE-X AUTISTIC PATIENTS | 1 | 3 |
| 1505 | 3 | 6 | 232 1984 PRENATAL DIAGNOSIS 4(6):473-474 VENTER PA; COETZEE DJ; BADENHORST A; MARX MP; HOF JO; BEHARI D; WILMOT J; BATTSON SA A CONFIRMED PRENATAL-DIAGNOSIS OF A FEMALE FETUS WITH THE FRAGILE X-CHROMOSOME | 1 | 4 |
| 1506 | 3 | 6 | 267 1985 CLINICAL GENETICS 28(5):399-400 SOUDEK D DECREASE OF FRAGILE X-FREQUENCY IN STORED-BLOOD SAMPLES - INDIVIDUAL VARIABILITY | 1 | 1 |
| 1507 | 1 | 6 | 301 1985 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 24(2):239-240 HAGERMAN RJ; JACKSON AW AUTISM OR FRAGILE-X SYNDROME | 0 | 1 |
| 1508 | 2 | 6 | 350 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):611-617 JACOBS PA; SHERMAN S; TURNER G; WEBB T THE FRAGILE(X) SYNDROME - THE MUTATION PROBLEM | 14 | 19 |
| 1509 | 2 | 6 | 369 1986 BULLETIN OF EXPERIMENTAL BIOLOGY AND MEDICINE 102(12):1742-1745 ZAKHAROV AF; BEDELBAEVA KA; BARANOVSKAYA LI VARIABILITY OF FRAGILE X-CHROMOSOME EXPRESSION IN CONSECUTIVE CELL GENERATIONS | 0 | 0 |
| 1510 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1511 | 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 |
| 1512 | 2 | 6 | 683 1990 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 163(5):1713-1714 SINDWANI V; VERMA RS CYTOGENETIC UNCERTAINTIES SURROUNDING THE FRAGILE X IN MARTIN-BELL SYNDROME | 0 | 0 |
| 1513 | 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 |
| 1514 | 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 |
| 1515 | 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 |
| 1516 | 4 | 6 | 927 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):170-173 SHAPIRO LR; WILMOT PL; FISCH GS PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME IN AMNIOTIC-FLUID - CALCULATION OF ACCURACY | 1 | 1 |
| 1517 | 4 | 6 | 944 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):328-332 NOLIN SL; SNIDER DA; JENKINS EC; DOBKIN CS; PATCHELL K; KRAWCZUN M; STRONG G; COLWELL M; VICTOR A; PAYYAPILLI T; TURCZYN M; LITTLE A; NAGARAJA U; DOYLE N; KENEFICK B; SULLIVAN C NEW-YORK-STATE SCREENING-PROGRAM FOR FRAGILE-X SYNDROME - A PROGRESS REPORT | 7 | 8 |
| 1518 | 3 | 6 | 1166 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):374-377 STEYAERT J; BORGHGRAEF M; FRYNS JP APPARENTLY ENHANCED VISUAL INFORMATION-PROCESSING IN FEMALE FRAGILE-X CARRIERS - PRELIMINARY FINDINGS | 1 | 1 |
| 1519 | 4 | 6 | 1214 1994 GENETIC COUNSELING 5(4):377-380 WIEGERS AM; CURFS LMG; MEIJER H; OOSTRA B; FRYNS JP A DELETION OF 1.6 KB PROXIMAL TO THE CGG REPEAT OF THE FMR1-GENE CAUSES FRAGILE X-LIKE PSYCHOLOGICAL FEATURES | 0 | 0 |
| 1520 | 1 | 6 | 1245 1994 KLINISCHE PADIATRIE 206(5):410-411 FEHLOW P; MIOSGE W; WALTHER F ASSOCIATION OF SAETHRE-CHOTZEN-SYNDROME AND FRAGILE-X-SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1521 | 2 | 6 | 1311 1995 BONE MARROW TRANSPLANTATION 16(4):625-626 MORTON J; ARNOLD L; FLETCHER B; MCCARTHY C; ROWELL J; DURRANT S ALLOGENEIC BMT FROM A DONOR WITH FRAGILE-X SYNDROME - CYTOGENETIC AND MOLECULAR EVALUATION | 0 | 0 |
| 1522 | 4 | 6 | 1441 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):377-377 HowardPeebles PN Successful pregnancy in a fragile X carrier by donor egg | 2 | 3 |
| 1523 | 3 | 6 | 1736 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):322-325 Allingham-Hawkins SJ; Babul-Hirji R; Chitayat D; Holden JJA; Yang KT; Lee C; Hudson R; Gorwill H; Nolin SL; Glicksman A; Jenkins EC; Brown WT; Howard-Peebles PN; Becchi C; Cummings E; Fallon L; Seitz S; Black SH; Vianna-Morgante AM; Costa SS; Otto PA; Mingroni-Netto RC; Murray A; Webb J; MacSwinney F; Dennis N; Jacobs PA; Syrrou M; Georgiou I; Patsalis PC; Uzielli MLG; Guarducci S; Lapi E; Cecconi A; Ricci U Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data | 10 | 19 |
| 1524 | 4 | 6 | 1737 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):326-326 Vianna-Morgante AM Twinning and premature ovarian failure in premutation fragile X carriers | 8 | 9 |
| 1525 | 3 | 6 | 1764 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 87(5):436-439 Einfeld S; Tonge B; Turner G Longitudinal course of behavioral and emotional problems in Fragile X syndrome | 5 | 5 |
| 1526 | 5 | 6 | 1810 1999 JOURNAL OF MEDICAL GENETICS 36(7):565-566 Moore SJ; Strain L; Cole GF; Miedzybrodzka Z; Kelly KF; Dean JCS Fragile X syndrome with FMR1 and FMR2 deletion | 1 | 3 |
| 1527 | 3 | 6 | 1893 2000 HUMAN GENETICS 107(2):195-196 Castellvi-Bel S; Fernandez-Burriel M; Rife M; Jimenez D; Mallolas J; Sanchez A; Ramos F; Mila M Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles | 1 | 2 |
| 1528 | 5 | 6 | 1937 2000 JOURNAL OF MOLECULAR DIAGNOSTICS 2(3):128-131 Daly TM; Rafii A; Martin RA; Zehnbauer BA Novel polymorphism in the FMR1 gene resulting in a "pseudodeletion" of FMR1 in a commonly used fragile X assay | 0 | 0 |
| 1529 | 3 | 6 | 1962 2000 PRENATAL DIAGNOSIS 20(10):854-855 Wilkin H; Tuohy J; Theewis W Prenatal diagnosis of fragile X and Turner mosaicism in a 12-week fetus | 1 | 1 |
| 1530 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1531 | 4 | 6 | 2247 2003 BIOFUTUR (229):36-37 Nourrit F Fragile X and interference. | 0 | 0 |
| 1532 | 4 | 6 | 2254 2003 CLINICAL GENETICS 64(1):54-56 Rogers C; Partington MW; Turner GM Tremor, ataxia and dementia in older men may indicate a carrier of the fragile X syndrome | 3 | 3 |
| 1533 | 3 | 6 | 2322 2004 BRAIN AND COGNITION 54(3):235-239 Cornish K; Swainson R; Cunnington R; Wilding J; Morris P; Jackson G Do women with fragile X syndrome have problems in switching attention: Preliminary findings from ERP and fMRI | 0 | 0 |
| 1534 | 2 | 6 | 2334 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(24):2945-2946 Hagerman PJ; Hagerman RJ; Gane LW Genetic counseling for families of patients with fragile X syndrome - In reply | 0 | 0 |
| 1535 | 1 | 5 | 58 1982 HOSPITAL PRACTICE 17(7):17-& BROWN WT; JENKINS EC FRAGILE X - ITS DETECTABILITY | 1 | 1 |
| 1536 | 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 |
| 1537 | 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 |
| 1538 | 4 | 5 | 106 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):795-796 DAKER MG FRAGILE X-CHROMOSOME IN NORMAL MALES | 2 | 4 |
| 1539 | 1 | 5 | 253 1985 AMERICAN JOURNAL OF PUBLIC HEALTH 75(7):715-716 MILUNSKY A AN IMPORTANT CLINICAL APPROACH IN DETECTING THE FRAGILE X-SYNDROME | 0 | 1 |
| 1540 | 2 | 5 | 270 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):606-606 CONNOR JM; COLGAN JM; CROSSLEY JA; IMRIE SJ; YATES JRW; SHIACH C; HANN IM; FORBES CD MULTIPOINT LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE X-SYNDROME AND FAMILIES WITH HEMOPHILIA-B | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1541 | 1 | 5 | 271 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):612-612 DAVIES KE; HARPER K; MATTEI MG; MATTEI JF; VEENEMA H; TOMMERUP N; NIELSEN KB; MIKKELSEN M; BEIGHTON P; PEMBREY ME LINKAGE RELATIONSHIP OF DNA SEGMENT 52A (HGM7-DXS51) AND FACTOR-IX (HGM7-F9) TO FRAGILE-X MENTAL-RETARDATION (FRAXQ27) | 0 | 0 |
| 1542 | 0 | 5 | 273 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):653-653 HOLDEN JJA; MULLIGAN LM; FORSTERGIBSON C; SIMPSON NE; WHITE BN; OBERLE I; WROGEMANN K APPLICATION OF FLANKING DNA PROBES TO CARRIER DETECTION IN THE FRAGILE-X SYNDROME | 0 | 2 |
| 1543 | 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 |
| 1544 | 0 | 5 | 346 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):557-562 UCHIDA IA; FREEMAN VCP; BASRUR PK THE FRAGILE-X IN CATTLE | 4 | 20 |
| 1545 | 3 | 5 | 373 1986 CLINICAL GENETICS 29(2):95-95 DEARCE MA; HECHT F; SUTHERLAND GR; WEBB GC GUIDELINES FOR THE DIAGNOSIS OF FRAGILE X | 0 | 2 |
| 1546 | 4 | 5 | 378 1986 CLINICAL GENETICS 30(4):346-347 SOUDEK D FRAGILE-X - EXPERIENCE OF A LABORATORY | 3 | 3 |
| 1547 | 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 |
| 1548 | 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 |
| 1549 | 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 |
| 1550 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1551 | 1 | 5 | 654 1989 LANCET 2(8657):279-279 SCHEPIS C; PALAZZO R; RAGUSA RM; SPINA E; BARLETTA C ASSOCIATION OF CUTIS VERTICIS GYRATA WITH FRAGILE-X SYNDROME AND FRAGILITY OF CHROMOSOME-12 | 0 | 11 |
| 1552 | 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 |
| 1553 | 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 |
| 1554 | 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 |
| 1555 | 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 |
| 1556 | 2 | 5 | 924 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):161-161 HOWARDPEEBLES PN EFFECT OF DIALYZED SERA ON FRAGILE-X EXPRESSION | 0 | 0 |
| 1557 | 5 | 5 | 946 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):339-344 VIANNAMORGANTE AM; OTTO PA NOTES ON THE POPULATION-GENETICS OF FRAGILE X SYNDROME | 1 | 1 |
| 1558 | 1 | 5 | 1224 1994 ITALIAN JOURNAL OF NEUROLOGICAL SCIENCES 15(7):365-368 MUSUMECI SA; ELIA M; FERRI R; SCUDERI C; DELGRACCO S EVOKED SPIKES AND GIANT SOMATOSENSORY-EVOKED POTENTIALS IN A PATIENT WITH FRAGILE-X SYNDROME | 3 | 8 |
| 1559 | 2 | 5 | 1246 1994 LANCET 344(8935):1500-1500 TURNER G; ROBINSON H; WAKE S; MARTIN N DIZYGOUS TWINNING AND PREMATURE MENOPAUSE IN FRAGILE-X SYNDROME | 31 | 50 |
| 1560 | 2 | 5 | 1295 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 57(3):508-509 LAXOVA R FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1561 | 2 | 5 | 1307 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(6):544-544 TURK J TREATMENT OF FRAGILE-X SYNDROME | 0 | 0 |
| 1562 | 4 | 5 | 1313 1995 BRAIN & DEVELOPMENT 17(5):322-322 NAKAHORI Y THE INCIDENCE OF THE FRAGILE-X SYNDROME IN JAPANESE - COMMENTARY ON NANBAS PAPER | 0 | 0 |
| 1563 | 2 | 5 | 1378 1995 LANCET 346(8970):309-310 CONWAY GS; HETTIARACHCHI S; MURRAY A; JACOBS PA FRAGILE-X PREMUTATIONS IN FAMILIAL PREMATURE OVARIAN FAILURE | 19 | 41 |
| 1564 | 2 | 5 | 1639 1998 ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE 152(1):89-90 Tsuchiya KD; Forsythe M; Robin NH; Tunnessen WW Picture of the month - Fragile X syndrome | 0 | 0 |
| 1565 | 0 | 5 | 1722 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(2):140-141 Hjalgrim H; Jacobsen TB; Norgaard K; Lou HC; Brondum-Nielsen K; Jonassen O Frontal-subcortical hypofunction in the fragile X syndrome | 5 | 6 |
| 1566 | 4 | 5 | 1746 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):202-203 Tuncbilek E; Alikasifoglu M; Boduroglu K; Aktas D; Anar B Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology | 3 | 3 |
| 1567 | 2 | 5 | 1806 1999 JOURNAL OF MEDICAL GENETICS 36(2):171-171 Macpherson J; Murray A; Webb J; Jacobs P Fragile X syndrome: of POF and premutations | 0 | 1 |
| 1568 | 4 | 5 | 1813 1999 MEDICAL JOURNAL OF AUSTRALIA 170(12):624-624 Cohen J; Loesch DZ Fragile X syndrome: do professionals know about it? | 0 | 0 |
| 1569 | 2 | 5 | 1939 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(2):264-266 Eliez S; Reiss AL Generics of childhood disorders: XI. Fragile X syndrome | 0 | 0 |
| 1570 | 1 | 5 | 1940 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(4):398-398 Levitas A Fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1571 | 0 | 5 | 1941 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(4):398-399 Lombroso PJ Fragile X syndrome - Dr. Lombroso replies | 0 | 0 |
| 1572 | 1 | 5 | 1963 2000 REVISTA DE NEUROLOGIA 30(10):996-997 Serrano-Castro PJ; Serrano-Castillo P A historical description of the association of macro-orchidea, mental retardation and cranial dysmorphia in males (fragile X chromosome syndrome) by A.B Richerand | 0 | 0 |
| 1573 | 2 | 5 | 2289 2003 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 42(5):516-517 Lung FW; Chen PJ Fragile X syndrome in adolescent prostitutes in southern Taiwan | 0 | 1 |
| 1574 | 3 | 5 | 2315 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 125A(3):320-320 Milunsky JM; Maher TA Fragile X carrier screening and spinocerebellar ataxia in older males | 0 | 0 |
| 1575 | 1 | 5 | 2331 2004 ISRAEL JOURNAL OF PSYCHIATRY AND RELATED SCIENCES 41(1):70-70 Kandil ST; Bilici M; Aksu HB; Celep F; Karaguzel A Early infantile autism and fragile X anomaly | 0 | 0 |
| 1576 | 2 | 4 | 16 1981 CLINICAL GENETICS 20(1):78-78 HOWARDPEEBLES PN FRAGILE-X CHROMOSOME IN NORMAL MALES | 4 | 7 |
| 1577 | 0 | 4 | 26 1981 LANCET 2(8254):1055-1055 BROWN WT; MEZZACAPPA PM; JENKINS EC SCREENING FOR FRAGILE X SYNDROME BY TESTICULAR SIZE MEASUREMENT | 16 | 23 |
| 1578 | 1 | 4 | 28 1981 LANCET 2(8258):1292-1292 JENKINS EC; BROWN WT; DUNCAN CJ; BROOKS J; BENYISHAY M; GIORDANO FM; NITOWSKY HM FEASIBILITY OF FRAGILE X-CHROMOSOME PRENATAL-DIAGNOSIS DEMONSTRATED | 56 | 77 |
| 1579 | 0 | 4 | 76 1982 LANCET 1(8263):101-101 GARDNER AP; HOWELL RT; MCDERMOTT A FRAGILE-X CHROMOSOME - CONSISTENT DEMONSTRATION OF FRAGILE SITE IN FIBROBLAST-CULTURES | 10 | 14 |
| 1580 | 2 | 4 | 111 1983 ANNALES DE GENETIQUE 26(3):147-149 CALVAMERCADO MP; MAUNOURY C; RETHORE MO; LEJEUNE J FRAGILE-X AND INHIBITION OF DIHYDROFOLATE-REDUCTASE - COMPARED EFFECTS OF 2 ANTIBIOTICS - TRIMETHOPRIME AND PYRIMETHAMINE | 6 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1581 | 1 | 4 | 128 1983 CLINICAL GENETICS 24(5):320-323 DEARCE MA TABLES FOR THE CYTOGENETIC STUDY OF FRAGILE X-CHROMOSOMES FOR DIAGNOSTIC PURPOSES | 11 | 17 |
| 1582 | 0 | 4 | 151 1983 LANCET 2(8364):1427-1427 KINNELL HG; BANU SP INSTITUTIONAL PREVALENCE OF FRAGILE X-SYNDROME | 5 | 8 |
| 1583 | 0 | 4 | 167 1984 AMERICAN JOURNAL OF HUMAN GENETICS 36(1):227-229 MIEZEJESKI CM; JENKINS EC; HILL AL; WISNIEWSKI K; BROWN WT VERBAL VS NONVERBAL ABILITY, FRAGILE-X SYNDROME, AND HETEROZYGOUS CARRIERS | 8 | 9 |
| 1584 | 0 | 4 | 175 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):209-214 RHOADS FA FRAGILE-X SYNDROME IN HAWAII - A SUMMARY OF CLINICAL-EXPERIENCE | 10 | 21 |
| 1585 | 0 | 4 | 218 1984 JOURNAL OF MEDICAL GENETICS 21(5):373-373 FITCHETT M; SEABRIGHT M DELETED X-CHROMOSOMES IN PATIENTS WITH THE FRAGILE X-SYNDROME | 10 | 14 |
| 1586 | 1 | 4 | 221 1984 LANCET 1(8370):220-220 WEBB T; THAKE A; TODD J; BUNDEY S PREVALENCE OF FRAGILE X-CHROMOSOME | 2 | 4 |
| 1587 | 2 | 4 | 222 1984 LANCET 1(8370):220-220 JANCAR J PREVALENCE OF FRAGILE X-CHROMOSOME | 1 | 3 |
| 1588 | 0 | 4 | 223 1984 LANCET 1(8370):220-221 LINNA SL; SIMILA S; HARO E; HERVA R PREVALENCE OF FRAGILE X-CHROMOSOME | 2 | 4 |
| 1589 | 0 | 4 | 275 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):726-726 PURRELLO M; ALHADEFF B; ROCCHI M; ARCHIDIACONO N; DRAYNA D; SINISCALCO M RELATIVE POSITIVE OF POLYMORPHIC DNA LOCI OF THE HUMAN X-CHROMOSOME LONG ARM SUBTELOMERIC REGION WITH RESPECT TO THE FRAGILE X SITE (FRAXQ27) | 1 | 4 |
| 1590 | 1 | 4 | 298 1985 JOURNAL OF MEDICAL GENETICS 22(5):397-397 WINTER RM; PEMBREY ME; DAVIES KE ANALYSIS OF LINKAGE DATA WITH FACTOR-IX CORROBORATES THE HYPOTHESIS THAT A PREMUTATION, FOLLOWED BY A RECOMBINATION EVENT, GENERATES THE FULL MUTATION IN FRAGILE X-LINKED MENTAL-RETARDATION | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1591 | 1 | 4 | 313 1986 AMERICAN JOURNAL OF DISEASES OF CHILDREN 140(4):327-327 BOWERS EJ FRAGILE-X SYNDROME AND LEARNING-DISABILITIES | 1 | 2 |
| 1592 | 4 | 4 | 343 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):527-530 TOMMERUP N; HOLMGREN G; STEINBACH P FRAGILE-X - CARRIER DETECTION IN PREGNANCY | 1 | 4 |
| 1593 | 2 | 4 | 376 1986 CLINICAL GENETICS 29(5):475-475 TOMMERUP N THE FRAGILE X-CHROMOSOME - PRENATAL-DIAGNOSIS | 1 | 3 |
| 1594 | 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 |
| 1595 | 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 |
| 1596 | 1 | 4 | 432 1987 BRITISH MEDICAL JOURNAL 295(6603):922-922 MCKINLEY MJ; NICOLAIDES KH; KEARNEY LU; HERON O FRAGILE-X SYNDROME | 1 | 3 |
| 1597 | 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 |
| 1598 | 4 | 4 | 485 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 BURD L THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1599 | 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 |
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