| 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 GCS.
Page 12: 1 (1246) 2 (77) 3 (47) 4 (34) 5 (25) 6 (19) 7 (14) 8 (11) 9 (9) 10 (7) 11 (5) 12 (4) 13 (3) 14 (2) 15 (1) 16 (1) 17 (0) 18 (0) 19 (0) 20 (0) 21 (0) 22 (0) 23 (0) 24 (0)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1101 | 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 |
| 1102 | 19 | 24 | 1153 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):281-293 SUTHERLAND GR; BROWN WT; HAGERMAN R; JENKINS E; LUBS H; MANDEL JL; NELSON D; NERI G; PARTINGTON MW; RICHARDS RI; STEVENSON R; TURNER G SIXTH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 3 | 4 |
| 1103 | 7 | 10 | 1180 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):463-465 RYYNANEN M; PULKKINEN L; KIRKINEN P; SAARIKOSKI S FRAGILE-X SYNDROME IN EAST FINLAND - MOLECULAR APPROACH TO GENETIC AND PRENATAL-DIAGNOSIS | 3 | 4 |
| 1104 | 11 | 13 | 1182 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):471-473 HALLEY D; VANDENOUWELAND A; DEELEN W; VERMA I; OOSTRA B STRATEGY FOR RELIABLE PRENATAL DETECTION OF NORMAL-MALE CARRIERS OF THE FRAGILE-X-SYNDROME | 3 | 4 |
| 1105 | 16 | 21 | 1255 1994 PRENATAL DIAGNOSIS 14(6):469-474 STRAIN L; PORTEOUS MEM; GOSDEN CM; ELLIS PM; NEILSON JP; BONTHRON DT PRENATAL-DIAGNOSIS OF FRAGILE-X-SYNDROME - MANAGEMENT OF THE MALE FETUS WITH A PREMUTATION | 3 | 4 |
| 1106 | 27 | 43 | 1305 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(1):3-5 TURK J FRAGILE-X SYNDROME | 2 | 4 |
| 1107 | 11 | 19 | 1308 1995 ARCHIVES OF MEDICAL RESEARCH 26:S77-S83 DiazGallardo MY; BarrosNunez P; Diaz CA; Hernandez A; GomezEspinel I; Leal CA; Fragoso R; Figuera L; GarciaCruz D; RamirezDuenas ML; Cantu JM Molecular characterization of the fragile-X syndrome in the Mexican population | 2 | 4 |
| 1108 | 46 | 131 | 1325 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):199-217 Binstock TC Fragile X and the amygdala: Cognitive, interpersonal, emotional, and neuroendocrine considerations | 4 | 4 |
| 1109 | 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 |
| 1110 | 19 | 43 | 1387 1995 PEDIATRIC RESEARCH 38(5):638-643 BERRYKRAVIS E; HICAR M; CIURLIONIS R REDUCED CYCLIC-AMP PRODUCTION IN FRAGILE-X SYNDROME - CYTOGENETIC AND MOLECULAR CORRELATIONS | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1111 | 15 | 34 | 1400 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):1-14 Tranebjaerg L; Lubs HA; Borghgraef M; Brown WT; Fisch G; Fryns JP; Hagerman R; Jacobs PA; Mandel JL; Mulley J; Oostra B; Schwartz C; Sherman S; Willard H; Willems P Seventh International Workshop on the Fragile X and X-linked Mental Retardation | 2 | 4 |
| 1112 | 3 | 18 | 1443 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):395-398 Piussan C; Mathieu M; Berquin P; Fryns JP Fragile X mutation and FG syndrome-like phenotype | 1 | 4 |
| 1113 | 10 | 25 | 1454 1996 ANNALS OF CLINICAL AND LABORATORY SCIENCE 26(4):323-328 Mark HFL; Bier JAB; Scola P The frequency of chromosomal abnormalities in patients referred for fragile X analysis | 1 | 4 |
| 1114 | 19 | 37 | 1455 1996 ARCHIVES DE PEDIATRIE 3(8):814-821 Mornet E; SimonBouy B Molecular biology of fragile X syndrome: Applications to genetic counselling and molecular diagnosis | 3 | 4 |
| 1115 | 4 | 138 | 1501 1996 MEDICAL HYPOTHESES 47(4):289-298 Fischer KM Genes for Prader Willi Syndrome Angelman syndrome and fragile X syndrome are homologous, with genetic imprinting and unstable trinucleotide repeats causing mental retardation, autism and aggression | 0 | 4 |
| 1116 | 8 | 13 | 1556 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 72(2):245-246 Healey SC; Duffy DL; Martin NG; Turner G Is fragile X syndrome a risk factor for dizygotic twinning? | 2 | 4 |
| 1117 | 2 | 23 | 1569 1997 ARCHIVES OF DISEASE IN CHILDHOOD 76(3):264-267 Corrigan N; Stewart M; Scott M; Fee F Fragile X, iron, and neurodevelopmental screening in 8 year old children with mild to moderate learning difficulties | 0 | 4 |
| 1118 | 4 | 11 | 1573 1997 BRITISH MEDICAL JOURNAL 315(7117):1174-1175 Barnicoat A Screening for fragile X syndrome: a model for genetic disorders? | 1 | 4 |
| 1119 | 39 | 64 | 1579 1997 CURRENT OPINION IN NEUROLOGY 10(2):142-147 Chakrabarti L; Davies KE Fragile X syndrome | 2 | 4 |
| 1120 | 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 |
| 1121 | 5 | 12 | 1614 1997 JOURNAL OF SPECIAL EDUCATION 31(3):362-376 Powell L; Houghton S; Douglas G Comparison of etiology-specific cognitive functioning profiles for individuals with fragile X and individuals with Down syndrome | 2 | 4 |
| 1122 | 7 | 35 | 1615 1997 JOURNAL OF THEORETICAL BIOLOGY 188(1):53-67 Bat O; Kimmel M; Axelrod DE Computer simulation of expansions of DNA triplet repeats in the fragile X syndrome and Huntington's disease | 1 | 4 |
| 1123 | 4 | 10 | 1630 1997 SOUTH AFRICAN MEDICAL JOURNAL 87(4):418-420 Goldman A; Krause A; Jenkins T Fragile X syndrome occurs in the South African black population | 2 | 4 |
| 1124 | 36 | 61 | 1723 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):221-236 Holden JJA; Percy M; Allingham-Hawkins D; Brown WT; Chiurazzi P; Fisch G; Gane L; Gunter C; Hagerman R; Jenkins EC; Kooy RF; Lubs HA; Murray A; Neri G; Schwartz C; Tranebjaerg L; Villard L; Willems PJ Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997 | 1 | 4 |
| 1125 | 3 | 7 | 1743 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):350-351 Faradz SMH; Buckley M; Tang LP; Leigh D; Holden JJA Molecular screening for fragile X syndrome among Indonesian children with developmental disability | 3 | 4 |
| 1126 | 4 | 36 | 1756 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):272-276 Currie JR; Brown WT KH domain-containing proteins of yeast: Absence of a fragile X gene homologue | 0 | 4 |
| 1127 | 21 | 38 | 1767 1999 ANNALES DE GENETIQUE 42(4):197-201 Arrieta I; Criado B; Martinez B; Telez M; Nunez T; Penagarikano O; Ortega B; Lostao CM A survey of fragile X syndrome in a sample from Spanish Basque country | 3 | 4 |
| 1128 | 34 | 44 | 1773 1999 CLINICAL GENETICS 55(5):346-351 Tassone F; Longshore J; Zunich J; Steinbach P; Salat U; Taylor AK Tissue-specific methylation differences in a fragile X premutation carrier | 2 | 4 |
| 1129 | 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 |
| 1130 | 16 | 32 | 1792 1999 HUMAN MUTATION 14(1):71-79 Panagopoulos I; Lassen C; Kristoffersson U; Aman P A methylation PCR approach for detection of fragile X syndrome | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1131 | 19 | 34 | 1801 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:314-324 York A; von Fraunhofer N; Turk J; Sedgwick P Fragile-X syndrome, Down's syndrome and autism: awareness and knowledge amongst special educators | 2 | 4 |
| 1132 | 8 | 22 | 1852 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 92(5):336-342 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Carrier testing in fragile X syndrome: Effect on self-concept | 2 | 4 |
| 1133 | 33 | 48 | 1863 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):183-188 Willemsen R; Oostra BA FMRP detection assay for the diagnosis of the fragile X syndrome | 1 | 4 |
| 1134 | 14 | 37 | 1866 2000 AMERICAN JOURNAL ON MENTAL RETARDATION 105(4):286-299 Kau ASM; Reider EE; Payne L; Meyer WA; Freund L Early behavior signs of psychiatric phenotypes in fragile X syndrome | 2 | 4 |
| 1135 | 16 | 20 | 1890 2000 GENETIC TESTING 4(3):289-292 Geva E; Yaron Y; Shomrat R; Ben-Yehuda A; Zabari S; Peretz H; Naiman T; Yeger H; Orr-Urtreger A The risk of Fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known Fragile X families | 3 | 4 |
| 1136 | 8 | 16 | 1912 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:81-85 Sabaratnam M Pathological and neuropathological findings in two males with fragile-X syndrome | 2 | 4 |
| 1137 | 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 |
| 1138 | 12 | 20 | 1947 2000 MOLECULAR AND CELLULAR PROBES 14(2):115-119 Mila M; Castellvi-Bel S; Sanchez A; Barcelo A; Badenas C; Mallolas J; Estivill X Rare variants in the promoter of the fragile X syndrome gene (FMR1) | 3 | 4 |
| 1139 | 0 | 0 | 1968 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):177-177 Hagerman RJ; Greco C; Chudley A; Leehey M; Tassone F; Grigsby J; Hills J; Wilson R; Harris SW; Hagerman PJ Neuropathology and neurodegenerative features in some older male premutation carriers of fragile X syndrome. | 3 | 4 |
| 1140 | 28 | 88 | 2001 2001 BRAIN RESEARCH BULLETIN 56(3-4):367-373 Grabczyk E; Kumari D; Usdin K Fragile X syndrome and Friedreich's ataxia: Two different paradigms for repeat induced transcript insufficiency | 0 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1141 | 6 | 21 | 2112 2002 CELLULAR & MOLECULAR BIOLOGY LETTERS 7(3):877-883 Denman RB Methylation of the arginine-glycine-rich region in the fragile X mental retardation protein FMRP differentially affects RNA binding | 2 | 4 |
| 1142 | 17 | 25 | 2119 2002 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 44(11):724-728 Berry-Kravis E Epilepsy in fragile X syndrome | 4 | 4 |
| 1143 | 15 | 32 | 2186 2002 NEUROPSYCHOLOGIA 40(8):1343-1349 Wilding J; Cornish K; Munir F Further delineation of the executive deficit in males with fragile-X syndrome | 4 | 4 |
| 1144 | 23 | 52 | 2194 2002 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 99(24):15758-15763 Qin M; Kang J; Smith CB Increased rates of cerebral glucose metabolism in a mouse model of fragile X mental retardation | 3 | 4 |
| 1145 | 15 | 28 | 2225 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 117A(1):21-29 Glaser B; Hessl D; Dyer-Friedman J; Johnston C; Wisbeck J; Taylor A; Reiss A Biological and environmental contributions to adaptive behavior in fragile X syndrome | 0 | 4 |
| 1146 | 28 | 58 | 2230 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 118B(1):81-88 Barnea-Goraly N; Eliez S; Hedeus M; Menon V; White CD; Moseley M; Reiss AL White matter tract alterations in fragile X syndrome: Preliminary evidence from diffusion tensor imaging | 0 | 4 |
| 1147 | 19 | 46 | 2231 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 121B(1):119-127 Aziz M; Stathopulu E; Callias M; Taylor C; Turk J; Oostra B; Willemsen R; Patton M Clinical features of boys with fragile X premutations and intermediate alleles | 0 | 4 |
| 1148 | 12 | 41 | 2250 2003 BRAIN RESEARCH 971(1):83-89 Galvez R; Gopal AR; Greenough WT Somatosensory cortical barrel dendritic abnormalities in a mouse model of the fragile X mental retardation syndrome | 2 | 4 |
| 1149 | 8 | 36 | 2303 2003 PEDIATRICS 111(2):407-416 Bailey DB; Skinner D; Sparkman KL Discovering fragile X syndrome: Family experiences and perceptions | 4 | 4 |
| 1150 | 0 | 0 | 6 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A99-A99 BRYANT EM; HOEHN H; MARTIN GM EXPRESSION OF THE FRAGILE X IN EUPLOID SOMATIC-CELL HYBRIDS | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1151 | 0 | 2 | 14 1981 CLINICAL GENETICS 19(2):140-141 SOUDEK D; GORZNY N NO FRAGILE X-CHROMOSOME IN NORMAL MEN | 1 | 3 |
| 1152 | 0 | 0 | 38 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A82-A82 BROWN T; JENKINS E; FRIEDMAN E; BROOKS J; DUNCAN C; COHEN I; HILL L; WISNIEWSKI K; FRENCH J A CONTROLLED TRIAL OF FOLIC-ACID THERAPY IN FRAGILE-X INDIVIDUALS | 3 | 3 |
| 1153 | 0 | 1 | 46 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A149-A149 WANG JC; BOSS GR; MAGNER MT; ERBE RW FOLATE PATHWAYS IN CELLS FROM FRAGILE-X SYNDROME PATIENTS AND CARRIERS | 2 | 3 |
| 1154 | 16 | 81 | 50 1982 ARCHIVES FRANCAISES DE PEDIATRIE 39(8):633-639 MATTEI JF FRAGILE X-LINKED MENTAL-RETARDATION | 3 | 3 |
| 1155 | 5 | 37 | 84 1982 WESTERN JOURNAL OF MEDICINE 137(4):278-281 MOORE BC; GLOVER TW; KAISERMCCAW B; HECHT F FRAGILE X-LINKED MENTAL-RETARDATION AND MACRO-ORCHIDISM | 1 | 3 |
| 1156 | 0 | 0 | 103 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A174-A174 HOLDEN J; BECKETT J; MULLIGAN L; PHILLIPS A; SIMPSON N; PARTINGTON M; HAMERTON J; WANG HS; DONALD L; WHITE B A SEARCH FOR RESTRICTION FRAGMENT LENGTH POLYMORPHISMS (RFLPS) LINKED TO THE FRAGILE-X FORM OF X-LINKED MENTAL-RETARDATION | 0 | 3 |
| 1157 | 1 | 1 | 118 1983 CLINICAL GENETICS 23(3):229-229 FONATSCH C FRAGILE X-CHROMOSOME IN FIBROBLASTS - LONGITUDINAL-STUDY ON TECHNICAL VARIATIONS | 3 | 3 |
| 1158 | 8 | 28 | 139 1983 IRISH JOURNAL OF MEDICAL SCIENCE 152(12):440-445 DEARCE MA; LAW E; MASTERSON JG NON-SPECIFIC X-LINKED MENTAL-RETARDATION WITH FRAGILE-X CHROMOSOME - SOMATIC FEATURES, CYTOGENETIC DIAGNOSIS AND ELEMENTS FOR GENETIC-COUNSELING | 1 | 3 |
| 1159 | 0 | 0 | 157 1983 PEDIATRIE 38(3):191-198 JALBERT P FRAGILE X-LINKED MENTAL-RETARDATION - MORE QUESTIONS | 1 | 3 |
| 1160 | 5 | 52 | 161 1983 SCHWEIZERISCHE MEDIZINISCHE WOCHENSCHRIFT 113(7):238-244 ZOLLINGER A; SCHMID W; VILAN J; SORG B; KNOBLAUCH M X-LINKED MENTAL-RETARDATION WITH FRAGILE X-CHROMOSOME AND MACROORCHIDISM | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1161 | 15 | 52 | 164 1984 ALABAMA JOURNAL OF MEDICAL SCIENCES 21(1):68-72 SCARBROUGH PR; COSPER P; FINLEY SC; SMITH NB FRAGILE-X SYNDROME - AN OVERVIEW | 0 | 3 |
| 1162 | 1 | 2 | 181 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):275-276 HOWARDPEEBLES PN; CARROLL AJ RECOMBINATION BETWEEN THE FRAGILE-X AND G6PD | 1 | 3 |
| 1163 | 0 | 0 | 198 1984 CYTOGENETICS AND CELL GENETICS 37(1-4):587-587 SNYDER FF; LIN CC; HARASYM CA; JAMRO HK; KUSHNIG ML; LOWE JK; OBRIEN SI EVIDENCE FOR CLOSE ASSOCIATION BETWEEN THE FRAGILE X(Q27-28)- CHROMOSOME SITE AND GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD) BUT NOT WITH HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE (HPRT) | 3 | 3 |
| 1164 | 0 | 3 | 208 1984 JOURNAL DE GENETIQUE HUMAINE 32(3):193-197 CRIPPA L; DELOZIERBLANCHET CD; ENGEL E STUDIES OF THE CYTOGENETIC VARIATIONS OF THE FRAGILE-X (FRA-X) ACCORDING TO CASES AND METHODS | 0 | 3 |
| 1165 | 7 | 8 | 209 1984 JOURNAL DE GENETIQUE HUMAINE 32(3):199-207 GILGENKRANTZ S; BOUE J; GREGOIRE MJ; TEJADA I MENTAL-RETARDATION AND (FRA-X) FRAGILE-X CHROMOSOME | 0 | 3 |
| 1166 | 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 |
| 1167 | 0 | 0 | 216 1984 JOURNAL OF MEDICAL GENETICS 21(4):298-298 WEBB TP; BUNDEY SE; THAKE A; TODD J STUDY OF THE FRAGILE X-CHROMOSOME AND MENTAL-RETARDATION | 0 | 3 |
| 1168 | 2 | 4 | 222 1984 LANCET 1(8370):220-220 JANCAR J PREVALENCE OF FRAGILE X-CHROMOSOME | 1 | 3 |
| 1169 | 3 | 7 | 236 1985 ACTA PAEDIATRICA SCANDINAVICA 74(6):974-974 FLOOD A; SANNER G REFRACTIVE ERRORS IN THE FRAGILE-X SYNDROME | 3 | 3 |
| 1170 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1171 | 7 | 13 | 248 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 22(2):415-416 BARBI G; STEINBACH P FRAGILE-X AND MARTIN-BELL SYNDROME - NEW SOURCE OF INFORMATION | 1 | 3 |
| 1172 | 7 | 19 | 249 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 22(3):571-575 MITCHELL JA; WRAY J; MICHALSKI K NEUROFIBROMATOSIS AND FRAGILE-X SYNDROME IN THE SAME PATIENT | 2 | 3 |
| 1173 | 4 | 17 | 316 1986 AMERICAN JOURNAL OF HUMAN GENETICS 38(4):533-539 ABRUZZO MA; HUNT PA; MAYER M; JACOBS PA; WANG JCC; ERBE RW A COMPARISON OF FRAGILE X-EXPRESSION IN LYMPHOCYTE AND LYMPHOBLASTOID CULTURES | 2 | 3 |
| 1174 | 5 | 16 | 341 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):475-481 JENKINS EC; KASTIN BR; KRAWCZUN MS; LELE KP; SILVERMAN WP; BROWN WT FRAGILE-X CHROMOSOME FREQUENCY IS CONSISTENT TEMPORALLY AND WITHIN REPLICATE CULTURES | 2 | 3 |
| 1175 | 0 | 10 | 358 1986 ANNALES DE GENETIQUE 29(4):261-263 BELGHITI D; RAZAVIENCHA F; RAOUL O; HIRBEC G; GUILLOT F; REINERT P; SOBEL A COINCIDENCE OF FAMILIAL SYSTEMIC LUPUS-ERYTHEMATOSUS AND THE FRAGILE-X SYNDROME | 0 | 3 |
| 1176 | 2 | 4 | 376 1986 CLINICAL GENETICS 29(5):475-475 TOMMERUP N THE FRAGILE X-CHROMOSOME - PRENATAL-DIAGNOSIS | 1 | 3 |
| 1177 | 4 | 5 | 378 1986 CLINICAL GENETICS 30(4):346-347 SOUDEK D FRAGILE-X - EXPERIENCE OF A LABORATORY | 3 | 3 |
| 1178 | 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 |
| 1179 | 1 | 4 | 432 1987 BRITISH MEDICAL JOURNAL 295(6603):922-922 MCKINLEY MJ; NICOLAIDES KH; KEARNEY LU; HERON O FRAGILE-X SYNDROME | 1 | 3 |
| 1180 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1181 | 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 |
| 1182 | 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 |
| 1183 | 3 | 9 | 516 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):143-147 NIELSEN KB GROWTH-PATTERN IN BOYS WITH FRAGILE-X | 3 | 3 |
| 1184 | 3 | 4 | 528 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):369-376 SANFILIPPO S; RAGUSA RM; SCILLATO F; RUGGERI M; NERI G FRAGILE-X EXPRESSION IN NORMAL AND MENTALLY-RETARDED SUBJECTS - EFFECT OF TREATMENT WITH AN ANTIFOLIC AGENT | 0 | 3 |
| 1185 | 21 | 49 | 534 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):435-442 KRAWCZUN MS; JENKINS EC; BROWN WT; SILVERMAN WP FRAGILE-X EXPRESSION IN SHORT-TERM WHOLE-BLOOD CULTURES IS AFFECTED BY CELL-DENSITY | 2 | 3 |
| 1186 | 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 |
| 1187 | 3 | 4 | 553 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):733-734 WILSON DP; CARPENTER NJ; BERKOVITZ G THYROID-FUNCTION IN MEN WITH FRAGILE X-LINKED MR | 3 | 3 |
| 1188 | 5 | 31 | 567 1988 CANCER 62(11):2383-2386 CUNNINGHAM M; DICKERMAN JD FRAGILE-X SYNDROME AND ACUTE LYMPHOBLASTIC-LEUKEMIA | 3 | 3 |
| 1189 | 2 | 19 | 568 1988 CHROMOSOMA 96(5):391-396 SAVAGE JRK; FITCHETT M THE BEHAVIOR OF FRAGILE-X AND OTHER ABERRATIONS DURING RECOVERY FROM LOW FOLATE CONDITIONS | 0 | 3 |
| 1190 | 17 | 31 | 572 1988 CLINICAL GENETICS 33(6):410-417 VEENEMA H; BEVERSTOCK GC; DEKONING T; PEARSON PL; VANDEKAMP JJP THE FRAGILE X-CHROMOSOME - AN EVALUATION OF THE RESULTS IN A ROUTINE CYTOGENETIC LABORATORY IN THE PERIOD 1981-1986 | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1191 | 7 | 32 | 576 1988 CYTOGENETICS AND CELL GENETICS 47(4):177-180 HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M FRAGILE-X EXPRESSION IN THYMIDINE-PROTOTROPHIC AND AUXOTROPHIC HUMAN-MOUSE SOMATIC-CELL HYBRIDS UNDER LOW AND HIGH THYMIDYLATE STRESS CONDITIONS | 1 | 3 |
| 1192 | 20 | 37 | 578 1988 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 30(2):257-261 HO HZ; GLAHN TJ; HO JC THE FRAGILE-X SYNDROME | 2 | 3 |
| 1193 | 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 |
| 1194 | 1 | 11 | 599 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(4):681-685 TSAI LY; CROWE RR; PATIL SR; MURRAY J; QUINN J SEARCH FOR DNA MARKERS IN 2 AUTISTIC MALES WITH THE FRAGILE-X SYNDROME | 2 | 3 |
| 1195 | 4 | 10 | 614 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(6):977-978 FERRI R BRAIN-STEM AUDITORY EVOKED-POTENTIALS IN THE FRAGILE-X SYNDROME | 2 | 3 |
| 1196 | 4 | 53 | 624 1989 AMERICAN ZOOLOGIST 29(2):569-591 LAIRD CD FROM POLYTENE CHROMOSOMES TO HUMAN EMBRYOLOGY - CONNECTIONS VIA THE HUMAN FRAGILE-X SYNDROME | 1 | 3 |
| 1197 | 6 | 8 | 626 1989 ARCHIVES OF DISEASE IN CHILDHOOD 64(9):1223-1224 WINTER RM FRAGILE-X MENTAL-RETARDATION | 1 | 3 |
| 1198 | 0 | 0 | 633 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):982-982 DAHL N; MALMSTROM H; HAMMARSTROMHEEROMA K; WADELIUS C; GUSTAVSON KH; HOLMGREN G; PETTERSSON U ISOLATION OF A NEW DNA MARKER TIGHTLY LINKED TO THE FRAGILE-X LOCUS (FRAXA) | 0 | 3 |
| 1199 | 0 | 1 | 720 1990 LANCET 336(8723):1131-1131 TEMPLE IK; BARAITSER M; PEMBREY ME; BUTLER L; JACOBS P; DAVIES KE UNUSUAL PRESENTATION OF FRAGILE-X SYNDROME | 2 | 3 |
| 1200 | 16 | 20 | 797 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):349-353 CARPENTER NJ; THIBODEAU SN; BROWN WT LINKAGE RELATIONSHIPS BETWEEN DXS105, DXS98, AND OTHER POLYMORPHIC DNA MARKERS FLANKING THE FRAGILE-X LOCUS | 2 | 3 |
Page 12: 1 (1246) 2 (77) 3 (47) 4 (34) 5 (25) 6 (19) 7 (14) 8 (11) 9 (9) 10 (7) 11 (5) 12 (4) 13 (3) 14 (2) 15 (1) 16 (1) 17 (0) 18 (0) 19 (0) 20 (0) 21 (0) 22 (0) 23 (0) 24 (0)
Generated by: HistCite(Vlad).
Version: 2004.08.24