| Missing Links? Citation Matrix | Graphs | Glossary HistCite Guide About |
Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by journal name.
Page 19: 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 |
|---|---|---|---|---|---|
| 1801 | 3 | 10 | 992 1992 JOURNAL OF MEDICAL GENETICS 29(8):599-599 TIZZANO EF; BAIGET M HIGH PROPORTION OF TWINS IN CARRIERS OF FRAGILE X-SYNDROME | 3 | 4 |
| 1802 | 7 | 8 | 993 1992 JOURNAL OF MEDICAL GENETICS 29(10):726-729 TARLETON J; WONG S; HEITZ D; SCHWARTZ C DIFFICULT DIAGNOSIS OF THE FRAGILE X-SYNDROME MADE POSSIBLE BY DIRECT DETECTION OF DNA MUTATIONS | 1 | 1 |
| 1803 | 23 | 34 | 994 1992 JOURNAL OF MEDICAL GENETICS 29(11):794-801 HEITZ D; DEVYS D; IMBERT G; KRETZ C; MANDEL JL INHERITANCE OF THE FRAGILE-X SYNDROME - SIZE OF THE FRAGILE-X PREMUTATION IS A MAJOR DETERMINANT OF THE TRANSITION TO FULL MUTATION | 72 | 108 |
| 1804 | 8 | 9 | 995 1992 JOURNAL OF MEDICAL GENETICS 29(12):919-920 TARLETON J; WONG S; SCHWARTZ C DIRECT ANALYSIS OF THE FMR-1 GENE PROVIDES AN EXPLANATION FOR AN EXCEPTIONAL CASE OF A FRAGILE-X NEGATIVE, MENTALLY-RETARDED MALE IN A FRAGILE-X FAMILY | 1 | 2 |
| 1805 | 10 | 13 | 1114 1993 JOURNAL OF MEDICAL GENETICS 30(2):94-96 SMITS APT; DREESEN JCFM; POST JG; SMEETS DFCM; DEDIESMULDERS C; SPAANSVANDERBIJL T; GOVAERTS LCP; WARREN ST; OOSTRA BA; VANOOST BA THE FRAGILE-X SYNDROME - NO EVIDENCE FOR ANY RECENT MUTATIONS | 27 | 34 |
| 1806 | 10 | 11 | 1115 1993 JOURNAL OF MEDICAL GENETICS 30(3):193-197 KNOBLOCH O; PELZ F; WICK U; NELSON DL; ZOLL B DIRECT VERSUS INDIRECT MOLECULAR DIAGNOSIS OF FRAGILE-X MENTAL-RETARDATION IN 40 GERMAN FAMILIES AT RISK | 1 | 1 |
| 1807 | 22 | 25 | 1116 1993 JOURNAL OF MEDICAL GENETICS 30(5):410-413 OOSTRA BA; JACKY PB; BROWN WT; ROUSSEAU F GUIDELINES FOR THE DIAGNOSIS OF FRAGILE-X SYNDROME | 45 | 60 |
| 1808 | 7 | 12 | 1117 1993 JOURNAL OF MEDICAL GENETICS 30(6):454-459 JACOBS PA; BULLMAN H; MACPHERSON J; YOUINGS S; ROONEY V; WATSON A; DENNIS NR POPULATION STUDIES OF THE FRAGILE-X - A MOLECULAR APPROACH | 46 | 79 |
| 1809 | 15 | 29 | 1118 1993 JOURNAL OF MEDICAL GENETICS 30(8):647-650 HIRST MC; KNIGHT SJL; CHRISTODOULOU Z; GREWAL PK; FRYNS JP; DAVIES KE ORIGINS OF THE FRAGILE-X SYNDROME MUTATION | 16 | 32 |
| 1810 | 10 | 27 | 1119 1993 JOURNAL OF MEDICAL GENETICS 30(9):761-766 DEVRIES BBA; FRYNS JP; BUTLER MG; CANZIANI F; WESBYVANSWAAY E; VANHEMEL JO; OOSTRA BA; HALLEY DJJ; NIERMEIJER MF CLINICAL AND MOLECULAR STUDIES IN FRAGILE-X PATIENTS WITH A PRADER-WILLI-LIKE PHENOTYPE | 18 | 33 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1811 | 7 | 9 | 1120 1993 JOURNAL OF MEDICAL GENETICS 30(9):785-787 SUZUMORI K; YAMAUCHI M; SEKI N; KONDO I; HORI T PRENATAL-DIAGNOSIS OF A HYPERMETHYLATED FULL FRAGILE-X MUTATION IN CHORIONIC VILLI OF A MALE FETUS | 1 | 4 |
| 1812 | 3 | 8 | 1234 1994 JOURNAL OF MEDICAL GENETICS 31(1):76-78 TEJADA MI; MORNET E; TIZZANO E; MOLINA M; BAIGET M; BOUE A IDENTIFICATION BY MOLECULAR DIAGNOSIS OF MOSAIC TURNERS-SYNDROME IN AN OBLIGATE CARRIER FEMALE FOR FRAGILE-X SYNDROME | 4 | 8 |
| 1813 | 0 | 0 | 1235 1994 JOURNAL OF MEDICAL GENETICS 31(2):170-170 STRAIN L; PORTEOUS MEM; BONTHRON DT PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - MANAGEMENT OF THE MALE FETUS WITH A PREMUTATION | 0 | 0 |
| 1814 | 0 | 0 | 1236 1994 JOURNAL OF MEDICAL GENETICS 31(2):173-173 BULLOCK S; LINDLEY V COMPLEMENTARY CYTOGENETIC AND MOLECULAR ANALYSIS OF A REFERRAL FOR FRAGILE-X TESTING | 0 | 0 |
| 1815 | 0 | 0 | 1237 1994 JOURNAL OF MEDICAL GENETICS 31(2):173-173 WANG Q; GREEN EP; MATHEW CG; BOBROW M NONRADIOACTIVE PCR BASED SCREENING FOR FRAGILE-X SYNDROME | 0 | 0 |
| 1816 | 1 | 3 | 1238 1994 JOURNAL OF MEDICAL GENETICS 31(3):260-261 GILLESSENKAESBACH G; HORSTHEMKE B CLINICAL AND MOLECULAR STUDIES IN FRAGILE-X PATIENTS WITH A PRADER-WILLI-LIKE PHENOTYPE | 0 | 3 |
| 1817 | 1 | 2 | 1239 1994 JOURNAL OF MEDICAL GENETICS 31(10):820-820 DEVRIES BBA; NIERMEIJER MF THE PRADER-WILLI-LIKE PHENOTYPE IN FRAGILE-X PATIENTS - A DESIGNATION FACILITATING CLINICAL (AND MOLECULAR) DIFFERENTIAL-DIAGNOSIS | 1 | 6 |
| 1818 | 6 | 12 | 1240 1994 JOURNAL OF MEDICAL GENETICS 31(12):950-952 CURTIS G; DENNIS N; MACPHERSON J THE IMPACT OF GENETIC-COUNSELING ON FEMALES IN FRAGILE-X FAMILIES | 1 | 1 |
| 1819 | 0 | 0 | 1367 1995 JOURNAL OF MEDICAL GENETICS 32(2):144-145 MORTON JE; RINDL PM; BULLOCK S; BUNDEY S; WEBB T FRAGILE-X SYNDROME IS LESS COMMON THAN PREVIOUSLY ESTIMATED | 1 | 2 |
| 1820 | 0 | 0 | 1368 1995 JOURNAL OF MEDICAL GENETICS 32(2):153-153 WANG Q; GREEN EP; BOBROW M; MATHEW CG SCREENING FOR THE FRAGILE-X A-MUTATION AND E-MUTATION BY AUTOMATED FLUORESCENT ANALYSIS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1821 | 0 | 0 | 1369 1995 JOURNAL OF MEDICAL GENETICS 32(2):153-153 BULLOCK S; LINDLEY VH; STEVENSON K; COLE T MOLECULAR DNA TESTING OF A FAMILY MANIFESTING FRAGILE-X SYNDROME IN BOTH THE FRAX-A FULL MUTATION AND MOSAIC FORMS | 0 | 0 |
| 1822 | 0 | 0 | 1370 1995 JOURNAL OF MEDICAL GENETICS 32(2):154-154 BULLOCK S; FELIX CA; BUTTERWORTH MA; STEVENSON K; WILLIAMS D THE USE OF MOLECULAR DNA TESTING TO DISTINGUISH BETWEEN MUTATIONS AT THE FRAGILE-X A-SITES AND E-SITES | 0 | 0 |
| 1823 | 10 | 20 | 1371 1995 JOURNAL OF MEDICAL GENETICS 32(3):170-173 WANG Q; GREEN E; BOBROW M; MATHEW CG A RAPID, NONRADIOACTIVE SCREENING-TEST FOR FRAGILE-X MUTATIONS AT THE FRAXA AND FRAXE LOCI | 15 | 27 |
| 1824 | 16 | 27 | 1372 1995 JOURNAL OF MEDICAL GENETICS 32(3):236-239 MACPHERSON JN; CURTIS G; CROLLA JA; DENNIS N; MIGEON B; GREWAL PK; HIRST MC; DAVIES KE; JACOBS PA UNUSUAL (CGG)(N) EXPANSION AND RECOMBINATION IN A FAMILY WITH FRAGILE-X AND DIGEORGE-SYNDROME | 3 | 11 |
| 1825 | 16 | 40 | 1373 1995 JOURNAL OF MEDICAL GENETICS 32(10):764-769 DEVRIES BBA; ROBINSON H; STOLTEDIJKSTRA I; GI CVTP; DIJKSTRA PF; VANDOOM J; HALLEY DJJ; OOSTRA BA; TURNER G; NIERMEIJER MF GENERAL OVERGROWTH IN THE FRAGILE-X SYNDROME - VARIABILITY IN THE PHENOTYPIC-EXPRESSION OF THE FMR1 GENE MUTATION | 6 | 15 |
| 1826 | 8 | 12 | 1374 1995 JOURNAL OF MEDICAL GENETICS 32(11):907-908 PINTADO E; DEDIEGO Y; HMADCHA A; CARRASCO M; SIERRA J; LUCAS M INSTABILITY OF THE CGG REPEAT AT THE FRAXA LOCUS AND VARIABLE PHENOTYPIC-EXPRESSION IN A LARGE FRAGILE-X PEDIGREE | 2 | 9 |
| 1827 | 13 | 35 | 1375 1995 JOURNAL OF MEDICAL GENETICS 32(12):925-929 KIRCHGESSNER CU; WARREN ST; WILLARD HF X INACTIVATION OF THE FMR1 FRAGILE-X MENTAL-RETARDATION GENE | 5 | 12 |
| 1828 | 10 | 13 | 1491 1996 JOURNAL OF MEDICAL GENETICS 33(4):338-340 Mila M; CastellviBel S; Sanchez A; Lazaro C; Villa M; Estivill X Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene | 9 | 15 |
| 1829 | 15 | 21 | 1492 1996 JOURNAL OF MEDICAL GENETICS 33(5):376-378 Wang ZM; Taylor AK; Bridge JA FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male | 17 | 22 |
| 1830 | 13 | 20 | 1493 1996 JOURNAL OF MEDICAL GENETICS 33(12):1007-1010 deVries BBA; Jansen CCAM; Duits AA; Verheij C; Willemsen R; vanHemel JO; vandenOuweland AMW; Niermeijer MF; Oostra BA; Halley DJJ Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family | 31 | 38 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1831 | 0 | 0 | 1602 1997 JOURNAL OF MEDICAL GENETICS 34:SP69-SP69 Webb J; Murray A; Conway G; Jacobs P Premature ovarian failure and fragile X | 0 | 0 |
| 1832 | 0 | 0 | 1603 1997 JOURNAL OF MEDICAL GENETICS 34:505-505 Brady AF; Suri M; Emerson J; Bell J; Chotai K; Singh H; Pocha M; Brueton LA Unusual X chromosome inactivation resulting in fragile X phenotype in a girl with a deletion on (X)(q26q27) | 0 | 0 |
| 1833 | 0 | 0 | 1604 1997 JOURNAL OF MEDICAL GENETICS 34:531-531 Cottrell S; Redmond E; McMahon C; Genet S; Barnicoat A Two deletions causing reversal to normal phenotype in fragile X syndrome. | 0 | 0 |
| 1834 | 0 | 0 | 1605 1997 JOURNAL OF MEDICAL GENETICS 34:539-539 Buckingham A; Bell JA; Payne SJ; Masters K; Emmerson J; Holder SE Recurrence of Turner's syndrome in a fragile-X family | 0 | 0 |
| 1835 | 0 | 0 | 1606 1997 JOURNAL OF MEDICAL GENETICS 34:541-541 Moore S; Dean JCS; Cole GF; Hamilton L; Kelly KF; Strain L; Warner J Fragile X Syndrome resulting from a deletion of the FMR1 gene | 0 | 0 |
| 1836 | 17 | 29 | 1607 1997 JOURNAL OF MEDICAL GENETICS 34(1):1-5 Morton JE; Bundey S; Webb TP; MacDonald F; Rindl PM; Bullock S Fragile X syndrome is less common than previously estimated | 25 | 45 |
| 1837 | 7 | 10 | 1608 1997 JOURNAL OF MEDICAL GENETICS 34(3):250-251 Willemsen R; Los F; Mohkamsing S; vandenOuweland A; Deelen W; Galjaard H; Oostra B Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: A new appraisal | 10 | 12 |
| 1838 | 0 | 1 | 1609 1997 JOURNAL OF MEDICAL GENETICS 34(4):350-350 Taylor AK FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male - Reply | 0 | 0 |
| 1839 | 1 | 2 | 1610 1997 JOURNAL OF MEDICAL GENETICS 34(4):350-350 Loesch DZ FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male | 1 | 1 |
| 1840 | 12 | 38 | 1611 1997 JOURNAL OF MEDICAL GENETICS 34(11):907-911 vanRijn MA; deVries BBA; Tibben A; vandenOuweland AMW; Halley DJJ; Niermeijer MF DNA testing for fragile X syndrome: implications for parents and family | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1841 | 10 | 15 | 1612 1997 JOURNAL OF MEDICAL GENETICS 34(11):924-926 Losekoot M; Hoogendoorn E; Olmer R; Jansen CCAM; Oosterwijk JC; vandenOuweland AMW; Halley DJJ; Warren ST; Willemsen R; Oostra BA; Bakker E Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus | 1 | 7 |
| 1842 | 27 | 51 | 1685 1998 JOURNAL OF MEDICAL GENETICS 35(2):103-111 Wohrle D; Salat U; Glaser D; Mucke J; Meisel-Stosiek M; Schindler D; Vogel W; Steinbach P Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats | 15 | 28 |
| 1843 | 134 | 197 | 1686 1998 JOURNAL OF MEDICAL GENETICS 35(7):579-589 de Vries BBA; Halley DJJ; Oostra BA; Niermeijer MF The fragile X syndrome | 28 | 50 |
| 1844 | 5 | 8 | 1687 1998 JOURNAL OF MEDICAL GENETICS 35(10):878-878 Jenkins T; Krause A Molecular evidence that fragile X syndrome occurs in the South African black population | 0 | 0 |
| 1845 | 0 | 0 | 1803 1999 JOURNAL OF MEDICAL GENETICS 36:S64-S64 Lazarau L; Warburton SA; Roberts CE; Hughes HE; Bartlett S; Meredith AL; Ravine D Fragile X syndrome carrier females with full mutations inherited from a normal transmitting male | 0 | 0 |
| 1846 | 0 | 0 | 1804 1999 JOURNAL OF MEDICAL GENETICS 36:S65-S65 Chotai K; Payne SJ A fragile-X male mosaic for normal, premutation and full mutation FMR-1 alleles | 0 | 0 |
| 1847 | 10 | 21 | 1805 1999 JOURNAL OF MEDICAL GENETICS 36(2):167-170 de Vries BBA; van den Boer-van den Berg HMA; Niermeijer MF; Tibben A Dilemmas in Counselling females with the fragile X syndrome | 0 | 1 |
| 1848 | 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 |
| 1849 | 0 | 0 | 1807 1999 JOURNAL OF MEDICAL GENETICS 36(2):171-172 De Vries BBA; Halley DJJ; Oostra BA; Niermeijer MF Fragile X syndrome: of POF and premutations | 0 | 0 |
| 1850 | 12 | 18 | 1808 1999 JOURNAL OF MEDICAL GENETICS 36(3):253-257 Helderman-van den Enden ATJM; Maaswinkel-Mooij PD; Hoogendoorn E; Willemsen R; Maat-Kievit JA; Losekoot M; Oostra BA Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities | 3 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1851 | 16 | 22 | 1809 1999 JOURNAL OF MEDICAL GENETICS 36(6):467-470 de Vries BBA; Mohkamsing S; van den Ouweland AMW; Mol E; Gelsema K; van Rijn M; Tibben A; Halley DJJ; Duivenvoorden HJ; Oostra BA; Niermeijer MF; Collaborative Fragile X Study Grp Screening for the fragile X syndrome among the mentally retarded: a clinical study | 2 | 8 |
| 1852 | 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 |
| 1853 | 0 | 0 | 1928 2000 JOURNAL OF MEDICAL GENETICS 37:S18-S18 Mandel JL The fragile X syndrome: from families to CGG expansions and FMR1 gene function | 0 | 0 |
| 1854 | 0 | 0 | 1929 2000 JOURNAL OF MEDICAL GENETICS 37:S20-S20 Fisher A; Macpherson JN; Dennis NR; Barber JCK Targeted testing for fragile X: an audit of the first year. | 0 | 0 |
| 1855 | 0 | 0 | 1930 2000 JOURNAL OF MEDICAL GENETICS 37:S44-S44 James T; Trigg A; Lindley VH; Fews GA; Roberts E; McKeown C; Davison EV An unexpected finding of fragile X (FRAXA) syndrome in a fetal blood sample referred for abnormalities on ultrasound scan | 0 | 0 |
| 1856 | 0 | 0 | 1931 2000 JOURNAL OF MEDICAL GENETICS 37:S66-S66 Lazarou LP; Myring J; Knight SJL; Gardner AP; Clarke A Fragile X (E) syndrome. How common is it? | 0 | 0 |
| 1857 | 0 | 0 | 1932 2000 JOURNAL OF MEDICAL GENETICS 37:S75-S75 Fratter C; Morsman A; Seller A Genetic analysis for Fragile X syndrome by fluorescent PCR | 0 | 0 |
| 1858 | 0 | 0 | 1933 2000 JOURNAL OF MEDICAL GENETICS 37:S78-S78 Chotai K; Buckingham AE; Bentley CM; Wycherley RJ; Payne SJ Fragile-X intermediate alleles - A clinical dilemma | 0 | 0 |
| 1859 | 21 | 36 | 1934 2000 JOURNAL OF MEDICAL GENETICS 37(1):77-79 Beresford RG; Tatlidil C; Riddell DC; Welch JP; Ludman MD; Neumann PE; Greer WL Absence of fragile X syndrome in Nova Scotia | 4 | 4 |
| 1860 | 12 | 16 | 1935 2000 JOURNAL OF MEDICAL GENETICS 37(8):603-604 Willemsen R; Olmer R; Otero YD; Oostra BA Twin sisters, monozygotic with the fragile X mutation, but with a different phenotype | 7 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1861 | 36 | 66 | 1936 2000 JOURNAL OF MEDICAL GENETICS 37(11):842-850 Salat U; Bardoni B; Wohrle D; Steinbach P Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations? | 2 | 5 |
| 1862 | 0 | 0 | 2036 2001 JOURNAL OF MEDICAL GENETICS 38:S39-S39 Moore C; Daly EM; Tassone F; Schmitz N; Hagerman P; Jacobs P; Davies K; Murphy KC; Murphy DGM Neuroanatomical effect of FMR1 gene mRNA in premutation carriers of Fragile X syndrome | 0 | 0 |
| 1863 | 0 | 0 | 2037 2001 JOURNAL OF MEDICAL GENETICS 38:S40-S40 Daly E; Moore CJ; Schmitz N; Jacobs P; Davies K; Murphy KC; Murphy DGM Premutation expansion of CGG triplet repeats affects brain; a study of Male Carriers of Fragile X Syndrome | 0 | 0 |
| 1864 | 0 | 0 | 2038 2001 JOURNAL OF MEDICAL GENETICS 38:S63-S63 Warburton S; Waters J; Davison V Targeted diagnostic testing for fragile X syndrome | 0 | 0 |
| 1865 | 0 | 0 | 2039 2001 JOURNAL OF MEDICAL GENETICS 38:S64-S64 Wakeling W; King W; Taylor R Chemiluminescence detection offers a safe, effective and convenient alternative to radioisotopic labelling of probes for detection of Fragile X syndrome and other single gene disorders | 0 | 0 |
| 1866 | 14 | 19 | 2040 2001 JOURNAL OF MEDICAL GENETICS 38(7):453-456 Tassone F; Hagerman RJ; Taylor AK; Hagerman PJ A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA | 13 | 19 |
| 1867 | 0 | 0 | 2154 2002 JOURNAL OF MEDICAL GENETICS 39:S73-S73 Bilgen T; Keser I; Mihci E; Tacoy S; Haspolat S; Luleci G Screening of the FMR1 gene (CCG)n expansion by expand long PCR in families with fragile X syndrome in antalya province. | 0 | 0 |
| 1868 | 0 | 0 | 2155 2002 JOURNAL OF MEDICAL GENETICS 39:S76-S76 Jani A; Hodsdon P; Churchley K; Crocker M; Stefanou E; Cranston T; Stewart H; Seller A An atypical week for the Oxford Fragile X service: Two interesting cases | 0 | 0 |
| 1869 | 0 | 0 | 2280 2003 JOURNAL OF MEDICAL GENETICS 40:S15-S15 Ennis S; Collins A; Morton NE SNP-based haplotypes and LD blocks in the fragile X region | 0 | 0 |
| 1870 | 0 | 0 | 2281 2003 JOURNAL OF MEDICAL GENETICS 40:S49-S49 Dalton A; Mills AC; Rigby A; Manly T; Hollis C; Turk J; Cornish K The neuropsychological phenotype of fragile X premutation males | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1871 | 0 | 0 | 2282 2003 JOURNAL OF MEDICAL GENETICS 40:S80-S80 Payne S; Powell CM Fragile-X intermediate alleles - instability and inconclusion | 0 | 0 |
| 1872 | 18 | 22 | 2283 2003 JOURNAL OF MEDICAL GENETICS 40(5):377-379 Willemsen R; Smits A; Severijnen LA; Jansen M; Jacobs A; De Bruyn E; Oostra B Predictive testing for cognitive functioning in female carriers of the fragile X syndrome using hair root analysis | 3 | 3 |
| 1873 | 28 | 41 | 2284 2003 JOURNAL OF MEDICAL GENETICS 40(7):535-539 de Vries BBA; Severijnen LA; Jacobs A; Olmer R; Halley DJJ; Oostra BA; Willemsen R FMRP expression studies in blood and hair roots in a fragile X family with methylation mosaics | 1 | 1 |
| 1874 | 10 | 15 | 2338 2004 JOURNAL OF MEDICAL GENETICS 41(4) Tassone F; Hagerman RJ; Garcia-Arocena D; Khandjian EW; Greco CM; Hagerman PJ Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome | 0 | 0 |
| 1875 | 10 | 16 | 2339 2004 JOURNAL OF MEDICAL GENETICS 41(4) Zhou Y; Law HY; Boehm CD; Yoon CS; Cutting GR; Ng ISL; Chong SS Robust fragile X (CGG)(n) genotype classification using a methylation specific triple PCR assay | 0 | 0 |
| 1876 | 18 | 28 | 1811 1999 JOURNAL OF MEDICAL SCREENING 6(2):70-76 Wildhagen MF; van Os TAM; Polder JJ; ten Kate LP; Habbema JDF Efficacy of cascade testing for fragile X syndrome | 3 | 5 |
| 1877 | 1 | 7 | 22 1981 JOURNAL OF MENTAL DEFICIENCY RESEARCH 25(DEC):253-& RICHARDS BW; SYLVESTER PE; BROOKER C FRAGILE X-LINKED MENTAL-RETARDATION - THE MARTIN-BELL SYNDROME | 36 | 55 |
| 1878 | 8 | 17 | 149 1983 JOURNAL OF MENTAL DEFICIENCY RESEARCH 27(SEP):211-226 NIELSEN KB DIAGNOSIS OF THE FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) - CLINICAL FINDINGS IN 27 MALES WITH THE FRAGILE SITE AT XQ28 | 18 | 26 |
| 1879 | 6 | 21 | 396 1986 JOURNAL OF MENTAL DEFICIENCY RESEARCH 30:27-39 GILLBERG C; PERSSON E; WAHLSTROM J THE AUTISM-FRAGILE-X SYNDROME (AFRAX) - A POPULATION-BASED STUDY OF 10 BOYS | 14 | 24 |
| 1880 | 6 | 45 | 397 1986 JOURNAL OF MENTAL DEFICIENCY RESEARCH 30:129-148 MADISON LS; GEORGE C; MOESCHLER JB COGNITIVE-FUNCTIONING IN THE FRAGILE-X SYNDROME - A STUDY OF INTELLECTUAL, MEMORY AND COMMUNICATION-SKILLS | 24 | 29 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1881 | 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 |
| 1882 | 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 |
| 1883 | 15 | 22 | 712 1990 JOURNAL OF MENTAL DEFICIENCY RESEARCH 34:67-73 WEBB T; CRAWLEY P; BUNDEY S FOLATE TREATMENT OF A BOY WITH FRAGILE-X SYNDROME | 2 | 5 |
| 1884 | 3 | 7 | 713 1990 JOURNAL OF MENTAL DEFICIENCY RESEARCH 34:81-86 COLLACOTT RA; DUCKETT DP; MATHEWS D; WARRINGTON JS; YOUNG ID DOWNS-SYNDROME AND FRAGILE-X SYNDROME IN A SINGLE PATIENT | 0 | 0 |
| 1885 | 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 |
| 1886 | 11 | 67 | 1376 1995 JOURNAL OF MOLECULAR BIOLOGY 254(4):638-656 KETTANI A; KUMAR RA; PATEL DJ SOLUTION STRUCTURE OF A DNA QUADRUPLEX CONTAINING THE FRAGILE-X SYNDROME TRIPLET REPEAT | 12 | 95 |
| 1887 | 6 | 39 | 1688 1998 JOURNAL OF MOLECULAR BIOLOGY 283(1):111-120 Mariappan SVS; Silks LA; Bradbury EM; Gupta G Fragile X DNA triplet repeats, (GCC)(n), form hairpins with single hydrogen-bonded cytosine center dot cytosine mispairs at the CpG sites: Isotope-edited nuclear magnetic resonance spectroscopy on (GCC)(n) with selective (15)N4-labeled cytosine bases | 4 | 16 |
| 1888 | 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 |
| 1889 | 2 | 11 | 219 1984 JOURNAL OF NERVOUS AND MENTAL DISEASE 172(9):549-551 KERBESHIAN J; BURD L; MARTSOLF J A FAMILY WITH FRAGILE-X SYNDROME | 7 | 20 |
| 1890 | 0 | 0 | 1494 1996 JOURNAL OF NEUROCHEMISTRY 67:S34-S34 Chen TA; Lu XF; Yi YH; Ho WKK Analysis of a CGG sequence at the FMR-1 locus in fragile X site by PCR-DGGE method. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1891 | 0 | 0 | 1495 1996 JOURNAL OF NEUROCHEMISTRY 67:S36-S36 Chen TA; Lu XF; Ilo WKK; Yi YH; Chen SQ; Chen Z Variation of the CGG repeat in FMR-1 gene in non retarded Chinese population and fragile X syndrome patients | 0 | 0 |
| 1892 | 0 | 0 | 2285 2003 JOURNAL OF NEUROCHEMISTRY 85:1-1 Huber KM Recent progress in understanding the neural mechanisms of Fragile X Syndrome | 0 | 0 |
| 1893 | 7 | 15 | 299 1985 JOURNAL OF NEUROGENETICS 2(3):231-237 FORSTERGIBSON CJ; MULLIGAN LM; PARTINGTON MW; SIMPSON NE; HOLDEN JJA; WHITE BN THE GENETIC-DISTANCE BETWEEN THE COAGULATION FACTOR-IX GENE AND THE LOCUS FOR THE FRAGILE-X SYNDROME - CLINICAL IMPLICATIONS | 13 | 23 |
| 1894 | 19 | 35 | 2286 2003 JOURNAL OF NEUROGENETICS 17(2-3):223-230 Major T; Culjkovic B; Stojkovic O; Gucscekic M; Lakic A; Romac S Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation | 0 | 0 |
| 1895 | 1 | 4 | 714 1990 JOURNAL OF NEUROLOGY 237(1):65-66 MUSUMECI SA; FERRI R; BERGONZI P THE SPECIFICITY OF THE CHARACTERISTIC SLEEP EEG PATTERN IN THE FRAGILE-X SYNDROME | 1 | 1 |
| 1896 | 6 | 25 | 300 1985 JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY 48(2):150-153 FINELLI PF; PUESCHEL SM; PADREMENDOZA T; OBRIEN MM NEUROLOGICAL FINDINGS IN PATIENTS WITH THE FRAGILE-X SYNDROME | 19 | 28 |
| 1897 | 0 | 0 | 2156 2002 JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY 61(5):450-450 Greco CM; Hagerman RJ; Tassone F; Chudley AE; Del Bigio MR; Jacquemont S; Leehey M; Hagerman PJ Neuronal and astrocytic intranuclear inclusions in Fragile X carriers with cerebellar tremor/ataxia and cognitive changes. | 0 | 0 |
| 1898 | 23 | 59 | 1613 1997 JOURNAL OF NEUROSCIENCE 17(5):1539-1547 Feng Y; Gutekunst CA; Eberhart DE; Yi H; Warren ST; Hersch SM Fragile X mental retardation protein: Nucleocytoplasmic shuttling and association with somatodendritic ribosomes | 71 | 131 |
| 1899 | 11 | 37 | 2340 2004 JOURNAL OF NEUROSCIENCE 24(11):2648-2655 Antar LN; Afroz R; Dictenberg JB; Carroll RC; Bassell GJ Metabotropic glutamate receptor activation regulates Fragile X mental retardation protein and Fmr1 mRNA localization differentially in dendrites and at synapses | 0 | 0 |
| 1900 | 38 | 97 | 2341 2004 JOURNAL OF NEUROSCIENCE 24(25):5798-5809 Michel CI; Kraft R; Restifo LL Defective neuronal development in the mushroom bodies of Drosophila Fragile X Mental Retardation 1 Mutants | 0 | 0 |
Page 19: 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)
Generated by: HistCite(Vlad).
Version: 2004.08.24