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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 19: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1801 | 17 | 39 | 2178 2002 NEUROBIOLOGY OF DISEASE 11(1):53-63 Schenck A; Van de Bor V; Bardoni B; Giangrande A Novel features of dFMR1, the Drosophila orthologue of the fragile X mental retardation protein | 3 | 3 |
| 1802 | 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 |
| 1803 | 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 |
| 1804 | 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 |
| 1805 | 0 | 1 | 741 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):75-75 SCHLESSINGER D; ZUCCHI I; NAGARAJA R; LITTLE RD; ABIDI F; FREIJE D; PILIA G; PORTA G; YOON JY; JOHNSON SK; PALMIERI G; MONTANARO V; ROMANO G; CASAMASSIMI A; CICCODICOLA A; DURSO M CLONING OF THE FRAGILE-X LOCUS IN THE CONTEXT OF YEAST ARTIFICIAL CHROMOSOME-BASED MAPPING OF XQ24-28 | 0 | 0 |
| 1806 | 0 | 0 | 262 1985 CLINICAL GENETICS 27(3):334-335 SCHMIDT A PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME | 2 | 4 |
| 1807 | 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 |
| 1808 | 1 | 1 | 1087 1993 CYTOGENETICS AND CELL GENETICS 64(3-4):187-187 SCHMIDT M X-CHROMOSOME INACTIVATION PATTERN IN INTERSTITIAL DELETIONS OF THE FRAGILE X-REGION | 0 | 0 |
| 1809 | 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 |
| 1810 | 1 | 4 | 1176 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):451-451 SCHMIDT M; ROBERTSON A; CRAWFORD M X INACTIVATION PATTERN IN INTERSTITIAL DELETIONS OF THE FRAGILE-X REGION | 0 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1811 | 19 | 25 | 1749 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):221-225 Schmucker B; Seidel J Mosaicism for a full mutation and a normal size allele in two fragile X males | 4 | 6 |
| 1812 | 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 |
| 1813 | 0 | 0 | 1054 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1757-1757 SCHORDERET DF; PILLET N; PESCIA G; THONNEY F A COMPOUND HETEROZYGOTE FEMALE DETECTED IN A FAMILY WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1814 | 10 | 23 | 1209 1994 CLINICAL GENETICS 45(4):175-180 SCHRANDERSTUMPEL C; GERVER WJ; MEYER H; ENGELEN J; MULDER H; FRYNS JP PRADER-WILLI-LIKE PHENOTYPE IN FRAGILE-X SYNDROME | 4 | 17 |
| 1815 | 15 | 32 | 1987 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(3):226-230 Schultz-Pedersen S; Hasle H; Olsen JH; Friedrich U Evidence of decreased risk of cancer in individuals with fragile X | 0 | 2 |
| 1816 | 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 |
| 1817 | 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 |
| 1818 | 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 |
| 1819 | 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 |
| 1820 | 0 | 3 | 1448 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 65(4):355-356 Seemanova E Fragile X syndrome in incestuous families | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1821 | 0 | 0 | 750 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):163-163 SEEMANOVA E; GOETZ P; SVOBODOVA M; LESNY I INCESTUOUS MATINGS IN FAMILIES WITH FRAGILE (X) SYNDROME | 0 | 0 |
| 1822 | 25 | 36 | 2251 2003 BRAIN RESEARCH 972(1-2):9-15 Segal M; Kreher U; Greenberger V; Braun K Is fragile X mental retardation protein involved in activity-induced plasticity of dendritic spines? | 0 | 1 |
| 1823 | 20 | 24 | 1229 1994 JAPANESE JOURNAL OF GENETICS 69(3):259-267 SEKI N; ISHIKIRIYAMA S; YAMAUCHI M; HORI T CYTOGENETIC AND MOLECULAR ANALYSIS OF DYNAMIC MUTATION ASSOCIATED WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1824 | 5 | 50 | 2335 2004 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 34(1):41-48 Seltzer MM; Abbeduto L; Krauss MW; Greenberg J; Swe A Comparison groups in autism family research: Down syndrome, fragile X syndrome, and schizophrenia | 0 | 0 |
| 1825 | 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 |
| 1826 | 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 |
| 1827 | 0 | 0 | 12 1981 CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES 8(2):191-191 SERGOVICH F; POZSONYI J; HINTON G RECENT ADVANCES IN MENTAL-RETARDATION THE FRAGILE X-CHROMOSOME | 1 | 0 |
| 1828 | 0 | 0 | 57 1982 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 24(2):252-253 SERGOVICH F; POZSONYI J; HINTON GG RECENT ADVANCES IN MENTAL-RETARDATION - THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1829 | 2 | 13 | 2043 2001 MOLECULAR AND CELLULAR ENDOCRINOLOGY 183:S77-S85 Sermon K; Seneca S; De Rycke M; Goossens V; Van de Velde H; De Vos A; Platteau P; Lissens W; Van Steirteghem A; Liebaers I PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome | 0 | 9 |
| 1830 | 0 | 0 | 1793 1999 HUMAN REPRODUCTION 14:235-235 Sermon K; Seneca S; Lissens W; De Vos A; Vandervorst M; Vanderfaellie A; Bonnefont JP; Van Steirteghem A; Liebaers I Preimplantation genetic diagnosis for fragile-X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1831 | 12 | 23 | 1821 1999 PRENATAL DIAGNOSIS 19(13):1223-1230 Sermon K; Seneca S; Vanderfaeillie A; Lissens W; Joris H; Vandervorst M; Van Steirteghem A; Liebaers I Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG | 2 | 26 |
| 1832 | 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 |
| 1833 | 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 |
| 1834 | 0 | 0 | 356 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 25(1):188-188 SHABTAI F; KLAR D; HART J; HALBRECHT I FRAGILE-X SYNDROME - A GENETIC OR AN INFECTIOUS-DISEASE | 0 | 0 |
| 1835 | 7 | 11 | 887 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1736-1738 SHAPIRO LR THE FRAGILE X-SYNDROME - A PECULIAR PATTERN OF INHERITANCE | 2 | 5 |
| 1836 | 0 | 0 | 847 1991 CYTOGENETICS AND CELL GENETICS 56(3-4):221-221 SHAPIRO LR; EALLONARDO SJ; WILMOT PL INTERNAL CONTROL FOR SUCCESSFUL INDUCTION OF THE FRAGILE X-CHROMOSOME - OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION ELIMINATED | 1 | 1 |
| 1837 | 0 | 0 | 892 1991 PEDIATRIC RESEARCH 29(4):A134-A134 SHAPIRO LR; EALLONARDO SJ; WILMOT PL OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION AND THE FRAGILE-X SYNDROME | 0 | 0 |
| 1838 | 0 | 0 | 41 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A110-A110 SHAPIRO LR; HASEN J; GORDON G; SOUTHREN AL; WILMOT PL; BRENHOLZ P TESTICULAR INSUFFICIENCY AND DISORDERED THYROID METABOLISM IN THE FRAGILE X-CHROMOSOME SYNDROME | 5 | 7 |
| 1839 | 0 | 0 | 32 1981 PEDIATRIC RESEARCH 15(4):569-569 SHAPIRO LR; KUHR MD; WILMOT PL MULTIPLE SIBLING MENTAL-RETARDATION AND THE IMPACT OF THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1840 | 0 | 0 | 9 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A122-A122 SHAPIRO LR; KUHR MD; WILMOT PL; LILIENTHAL ER; HIGGS LC MULTIPLE SIBLING MENTAL-RETARDATION AND THE IMPACT OF THE FRAGILE X-CHROMOSOME | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1841 | 0 | 0 | 768 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):292-292 SHAPIRO LR; PETRELLA R; EALLONARDO SJ; WILMOT PL RELIABILITY OF OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION AS AN INDICATION OF SUCCESSFUL INDUCTION OF THE FRAGILE-X CHROMOSOME | 0 | 0 |
| 1842 | 0 | 0 | 91 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A117-A117 SHAPIRO LR; SUMMA GM; WILMOT PL; GLOTH E SCREENING AND DETECTION OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 1843 | 0 | 0 | 727 1990 PEDIATRIC RESEARCH 27(4):A136-A136 SHAPIRO LR; WILMOT PL SPONTANEOUS FRAGILE-X CHROMOSOMES IN ROUTINE AMNIOTIC-FLUID CULTURE - THE X-CHROMOSOME COMMON FRAGILE SITE [(X) (Q27.2)] MISTAKEN FOR THE FRAGILE-X CHROMOSOME [(X) (Q27.3)] | 0 | 0 |
| 1844 | 0 | 0 | 754 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):231-231 SHAPIRO LR; WILMOT PL PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE X-SYNDROME - DETERMINATION OF ACCURACY | 1 | 1 |
| 1845 | 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 |
| 1846 | 0 | 0 | 971 1992 CYTOGENETICS AND CELL GENETICS 60(3-4):265-265 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 |
| 1847 | 1 | 3 | 73 1982 LANCET 1(8263):99-100 SHAPIRO LR; WILMOT PL; BRENHOLZ P; LEFF A; MARTINO M; HARRIS G; MAHONEY MJ; HOBBINS JC PRENATAL-DIAGNOSIS OF FRAGILE-X CHROMOSOME | 38 | 59 |
| 1848 | 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 |
| 1849 | 0 | 0 | 1284 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1676-1676 SHAPIRO LR; WILMOT PL; MARINELLO MJ NONINDUCED FRAGILE-X CHROMOSOMES DETECTED IN ROUTINE AMNIOTIC-FLUID CELL-CULTURE - DETERMINATION OF SIGNIFICANCE | 0 | 0 |
| 1850 | 4 | 11 | 815 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):453-455 SHAPIRO LR; WILMOT PL; MURPHY PD PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME - POSSIBLE END OF THE EXPERIMENTAL PHASE FOR AMNIOTIC-FLUID | 5 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1851 | 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 |
| 1852 | 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 |
| 1853 | 0 | 4 | 808 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):408-410 SHAPIRO LR; WILMOT PL; SHAPIRO DA; PETTERSEN IM; CASAMASSIMA AC CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME - EFFICIENCY, UTILIZATION, AND TRENDS | 3 | 3 |
| 1854 | 23 | 46 | 1882 2000 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 42(11):768-774 Sheldon L; Turk J Monozygotic boys with fragile X syndrome | 1 | 2 |
| 1855 | 1 | 1 | 302 1985 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 24(2):240-240 SHELL J; CAMPBELL M AUTISM OR FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 1856 | 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 |
| 1857 | 0 | 0 | 1405 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):19-19 Shen Y; Zhu N; Huang D; Wu GY Studies on fragile X syndrome in the Chinese. | 0 | 0 |
| 1858 | 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 |
| 1859 | 11 | 21 | 1290 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(5):991-993 SHERMAN SL THE HIGH PREVALENCE OF FRAGILE-X PREMUTATION CARRIER FEMALES - IS THIS FREQUENCY UNIQUE TO THE FRENCH-CANADIAN POPULATION | 7 | 14 |
| 1860 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1861 | 22 | 33 | 1864 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):189-194 Sherman SL Premature ovarian failure in the fragile X syndrome | 12 | 24 |
| 1862 | 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 |
| 1863 | 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 |
| 1864 | 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 |
| 1865 | 17 | 21 | 1420 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):256-260 Sherman SL; Meadows KL; Ashley AE Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females | 12 | 16 |
| 1866 | 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 |
| 1867 | 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 |
| 1868 | 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 |
| 1869 | 4 | 12 | 247 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 21(4):771-775 SHIMANUKI K; LIN MS; WILSON MG REDUCTION OF FRAGILE X-EXPRESSION IN BLOOD AFTER CRYOPRESERVATION | 1 | 3 |
| 1870 | 0 | 0 | 1560 1997 AMERICAN JOURNAL OF PATHOLOGY 151(5):G3-G3 Shrimpton AE; Hicks K; Lamberson CM Fragile X syndrome molecular detection. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1871 | 0 | 10 | 1658 1998 GENERAL HOSPITAL PSYCHIATRY 20(2):126-127 Silva JA; Ferrari MM; Leong GB Erotomania in a case of fragile-X syndrome | 0 | 1 |
| 1872 | 8 | 23 | 126 1983 CLINICAL GENETICS 23(6):436-440 SILVERMAN W; LUBIN R; JENKINS EC; BROWN WT THE STRENGTH OF ASSOCIATION BETWEEN FRAGILE(X) CHROMOSOME PRESENCE AND MENTAL-RETARDATION | 8 | 11 |
| 1873 | 0 | 0 | 1020 1993 AMERICAN FAMILY PHYSICIAN 47(5):1072-1073 SIMENSEN RJ FRAGILE-X SYNDROME | 0 | 0 |
| 1874 | 2 | 3 | 1066 1993 AMERICAN JOURNAL ON MENTAL RETARDATION 97(4):477-479 SIMENSEN RJ FRAGILE X-SYNDROME - DIAGNOSIS, TREATMENT, AND RESEARCH - HAGERMAN,RJ, SILVERMAN,AC | 0 | 0 |
| 1875 | 0 | 0 | 611 1989 AMERICAN FAMILY PHYSICIAN 39(5):185-193 SIMENSEN RJ; ROGERS RC FRAGILE-X SYNDROME | 1 | 1 |
| 1876 | 21 | 41 | 661 1989 PSYCHOLOGY IN THE SCHOOLS 26(4):380-389 SIMENSEN RJ; ROGERS RC SCHOOL-PSYCHOLOGY AND MEDICAL DIAGNOSIS - THE FRAGILE X-SYNDROME | 1 | 1 |
| 1877 | 0 | 0 | 984 1992 INTERNATIONAL JOURNAL OF PSYCHOLOGY 27(3-4):395-395 SIMENSEN RJ; SAUL RA; TARLETON JD; PHELAN MC NEUROPSYCHOLOGICAL FUNCTIONING IN FRAGILE X-SYNDROME AND MONOSOMY-X MOSAICISM - A CASE PRESENTATION | 0 | 0 |
| 1878 | 8 | 19 | 659 1989 PEDIATRICS 83(4):547-552 SIMKO A; HORNSTEIN L; SOUKUP S; BAGAMERY N FRAGILE X-SYNDROME - RECOGNITION IN YOUNG-CHILDREN | 28 | 31 |
| 1879 | 11 | 28 | 1450 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 67(1):77-80 Simon EW; Finucane BM Facial emotion identification in males with fragile X syndrome | 6 | 6 |
| 1880 | 2 | 14 | 1365 1995 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 39:326-330 SIMON EW; RAPPAPORT DA; PAPKA M; WOODRUFFPAK DS FRAGILE-X AND DOWNS-SYNDROME - ARE THERE SYNDROME-SPECIFIC COGNITIVE PROFILES AT LOW IQ LEVELS | 2 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1881 | 37 | 73 | 2010 2001 COGNITIVE NEUROPSYCHOLOGY 18(1):1-18 Simon JA; Keenan JM; Pennington BF; Taylor AK; Hagerman RJ Discourse processing in women with fragile X syndrome: Evidence for a deficit establishing coherence | 6 | 7 |
| 1882 | 5 | 11 | 320 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):171-178 SIMPSON NE DERMATOGLYPHIC INDEXES OF MALES WITH THE FRAGILE-X SYNDROME AND OF THE FEMALE HETEROZYGOTES | 6 | 10 |
| 1883 | 3 | 25 | 174 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):195-207 SIMPSON NE; NEWMAN BJ; PARTINGTON MW FRAGILE-X SYNDROME .3. DERMATOGLYPHIC STUDIES IN MALES | 10 | 16 |
| 1884 | 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 |
| 1885 | 0 | 0 | 1349 1995 EPILEPSIA 36:S244-S244 SINGH R; SUTHERLAND G; MANSON J SEIZURES WITH EPILEPTOGENIC EEG PATTERN IN 2 SISTERS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 1886 | 7 | 18 | 1798 1999 JOURNAL OF CHILD NEUROLOGY 14(2):108-112 Singh R; Sutherland GR; Manson J Partial seizures with focal epileptogenic electroencephalographic patterns in three related female patients with fragile-X syndrome | 1 | 1 |
| 1887 | 15 | 39 | 1206 1994 CELL 77(1):33-39 SIOMI H; CHOI MY; SIOMI MC; NUSSBAUM RL; DREYFUSS G ESSENTIAL ROLE FOR KH DOMAINS IN RNA-BINDING - IMPAIRED RNA-BINDING BY A MUTATION IN THE KH DOMAIN OF FMR1 THAT CAUSES FRAGILE-X SYNDROME | 64 | 254 |
| 1888 | 0 | 0 | 1029 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):40-40 SIOMI H; SIOMI MC; NUSSBAUM RL; DREYFUSS G THE PROTEIN PRODUCT OF THE FRAGILE X-GENE, FMR-1, HAS CHARACTERISTICS OF AN RNA-BINDING PROTEIN | 0 | 0 |
| 1889 | 15 | 56 | 1076 1993 CELL 74(2):291-298 SIOMI H; SIOMI MC; NUSSBAUM RL; DREYFUSS G THE PROTEIN PRODUCT OF THE FRAGILE-X GENE, FMR1, HAS CHARACTERISTICS OF AN RNA-BINDING PROTEIN | 117 | 315 |
| 1890 | 23 | 53 | 2171 2002 MOLECULAR AND CELLULAR BIOLOGY 22(24):8438-8447 Siomi MC; Higashijima K; Ishizuka A; Siomi H Casein kinase II phosphorylates the fragile X mental retardation protein and modulates its biological properties | 5 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1891 | 13 | 43 | 1346 1995 EMBO JOURNAL 14(11):2401-2408 SIOMI MC; SIOMI H; SAUER WH; SRINIVASAN S; NUSSBAUM RL; DREYFUSS G FXR1, AN AUTOSOMAL HOMOLOG OF THE FRAGILE-X MENTAL-RETARDATION GENE | 51 | 95 |
| 1892 | 16 | 57 | 1502 1996 MOLECULAR AND CELLULAR BIOLOGY 16(7):3825-3832 Siomi MC; Zhang Y; Siomi H; Dreyfuss G Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them | 48 | 98 |
| 1893 | 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 |
| 1894 | 16 | 30 | 1306 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(1):33-37 SLANEY SF; WILKIE AOM; HIRST MC; CHARLTON R; MCKINLEY M; POINTON J; CHRISTODOULOU Z; HUSON SM; DAVIES KE DNA TESTING FOR FRAGILE-X SYNDROME IN SCHOOLS FOR LEARNING-DIFFICULTIES | 12 | 20 |
| 1895 | 1 | 10 | 1964 2000 VETERINARNI MEDICINA 45(10-11):308-310 Slota E; Danielak-Czech B; Pietraszewska J; Kozubska-Sobocinska A Preliminary identification of the fragile X in two crossbred cows | 0 | 1 |
| 1896 | 2 | 2 | 990 1992 JOURNAL OF MEDICAL GENETICS 29(4):287-287 SMART RD FRAGILE X-SYNDROME - AS COMMON AS 1ST THOUGHT | 2 | 4 |
| 1897 | 18 | 21 | 1131 1993 MENTAL RETARDATION 31(5):279-283 SMITH SE COGNITIVE DEFICITS ASSOCIATED WITH FRAGILE-X SYNDROME | 2 | 3 |
| 1898 | 0 | 0 | 1350 1995 FASEB JOURNAL 9(6):A1324-A1324 SMITH SS; LAAYOUN A; BAKER DJ; KHO MR RECOGNITION OF TELOMERE-LIKE STRUCTURES FROM THE HUMAN C-HA-RAS GENE AND THE TRINUCLEOTIDE REPEAT OF THE FMR-1 GENE OF FRAGILE-X BY HUMAN DNA METHYLTRANSFERASE | 0 | 0 |
| 1899 | 2 | 44 | 1241 1994 JOURNAL OF MOLECULAR BIOLOGY 243(2):143-151 SMITH SS; LAAYOUN A; LINGEMAN RG; BAKER DJ; RILEY J HYPERMETHYLATION OF TELOMERE-LIKE FOLDBACKS AT CODON-12 OF THE HUMAN C-HA-RAS GENE AND THE TRINUCLEOTIDE REPEAT OF THE FMR-1 GENE OF FRAGILE-X | 10 | 54 |
| 1900 | 11 | 13 | 1187 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):497-500 SMITS A; SMEETS D; HAMEL B; DREESEN J; DEHAAN A; VANOOST B PREDICTION OF MENTAL STATUS IN CARRIERS OF THE FRAGILE-X MUTATION USING CGG REPEAT LENGTH | 13 | 16 |
Page 19: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
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