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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 14: 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 |
|---|---|---|---|---|---|
| 1301 | 5 | 30 | 1213 1994 GENETIC COUNSELING 5(2):129-139 MAES B; FRYNS JP; VANWALLEGHEM M; VANDENBERGHE H PERSONAL INDEPENDENCE OF ADULT MENTALLY-RETARDED MEN WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1302 | 1 | 1 | 1456 1996 ARCHIVES OF DISEASE IN CHILDHOOD 74(1):88-88 Magnay D; Morritt J; Waterston T Fragile X syndrome | 0 | 0 |
| 1303 | 0 | 0 | 891 1991 OPTOMETRY AND VISION SCIENCE 68(8):634-640 MAINO DM; WESSON M; SCHLANGE D; CIBIS G; MAINO JH OPTOMETRIC FINDINGS IN THE FRAGILE X-SYNDROME | 5 | 9 |
| 1304 | 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 |
| 1305 | 0 | 0 | 1580 1997 CYTOGENETICS AND CELL GENETICS 77(1-2):P250-P250 Malarchuk S; Li S; Wertelecki W; Bychkova A; Livshits L Analysis of patients with fragile X syndrome in Ukraine. | 0 | 0 |
| 1306 | 0 | 0 | 1981 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):669-669 Mallolas J; Badenas C; Rite M; Soler A; Borrell A; Sanchez A; Mila M Prospective study of molecular fragile X syndrome prenatal diagnosis. | 0 | 0 |
| 1307 | 0 | 0 | 1042 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):828-828 MALMGREN H; GUSTAVSON KH; HOLMGREN G; PETTERSSON U; DAHL N STRONG FOUNDER EFFECT FOR THE FRAGILE X-SYNDROME IN SWEDEN | 0 | 0 |
| 1308 | 18 | 21 | 956 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(6):830-833 MALMGREN H; GUSTAVSON KH; WAHLSTROM J; ARPIHENRIKSSON I; BENSCH J; PETTERSSON U; DAHL N INFANTILE-AUTISM FRAGILE-X - MOLECULAR FINDINGS SUPPORT GENETIC-HETEROGENEITY | 3 | 6 |
| 1309 | 15 | 17 | 937 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):268-278 MALMGREN H; STEENBONDESON ML; GUSTAVSON KH; SEEMANOVA E; HOLMGREN G; OBERLE I; MANDEL JL; PETTERSSON U; DAHL N METHYLATION AND MUTATION PATTERNS IN THE FRAGILE-X SYNDROME | 13 | 17 |
| 1310 | 22 | 42 | 1619 1997 NATURE GENETICS 15(2):165-169 Malter HE; Iber JC; Willemsen R; deGraaff E; Tarleton JC; Leisti J; Warren ST; Oostra BA Characterization of the full fragile X syndrome mutation in fetal gametes | 45 | 84 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1311 | 0 | 0 | 1051 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1435-1435 MALTER HE; KARICKHOFF L; TUCKER M; WIKER S; WRIGHT G; MORTON P; MASSEY JB; ELSNER C; WARREN ST SINGLE-CELL ANALYSIS OF THE REPEAT EXPANSION MUTATION ASSOCIATED WITH FRAGILE X-SYNDROME | 0 | 0 |
| 1312 | 0 | 0 | 1402 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):14-14 Malzac P; Biancalana V; Voelckel MA; Moncla A; Pellissier MC; Boccaccio I; Mandel JL; Mattei JF A rare example of a reverse mutation in a fragile X syndrome family. | 0 | 0 |
| 1313 | 19 | 27 | 1474 1996 EUROPEAN JOURNAL OF HUMAN GENETICS 4(1):8-12 Malzac P; Biancalana V; Voelckel MA; Moncla A; Pellissier MC; Boccaccio I; Mattei JF Unexpected inheritance of the (CGG)(n) trinucleotide expansion in a fragile X syndrome family | 4 | 6 |
| 1314 | 13 | 25 | 1519 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):195-201 Mandel JL The fragile X mental retardation syndrome: the FMR1 gene and its mutations | 0 | 0 |
| 1315 | 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 |
| 1316 | 9 | 45 | 381 1986 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 51:195-203 MANDEL JL; ARVEILER B; CAMERINO G; HANAUER A; HEILIG R; KOENIG M; OBERLE I GENETIC-MAPPING OF THE HUMAN X-CHROMOSOME - LINKAGE ANALYSIS OF THE Q26-Q28 REGION THAT INCLUDES THE FRAGILE X-LOCUS AND ISOLATION OF EXPRESSED SEQUENCES | 4 | 36 |
| 1317 | 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 |
| 1318 | 24 | 31 | 906 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):5-27 MANDEL JL; HAGERMAN R; FROSTER U; BROWN WT; JENKINS EC; JACOBS P; TURNER G; LUBS H; NERI G 5TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 5 | 8 |
| 1319 | 0 | 0 | 1921 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:380-380 Manjunatha KR; Chettn GK; Arathi R; Bhaskar RG; Nandini PM; Chandra S; Bhaskaran GS; Brahmachari V Fragile-X syndrome: Cytogenetics and molecular analysis of subjects from Indian population | 0 | 0 |
| 1320 | 16 | 20 | 1426 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):293-295 Mannermaa A; Pulkkinen L; Kajanoja E; Ryynanen M; Saarikoski S Deletion in the FMR1 gene in a fragile-X male | 8 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1321 | 0 | 0 | 2091 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):518-518 Maranduba CMC; Vianna-Morgante AM; Passos-Bueno MR P172H mutation in the TM4SF2 gene accounts for 1% of non-fragile X mental retardation in Brazilian patients. | 0 | 0 |
| 1322 | 0 | 24 | 5 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(5):752-761 MARENI C; MIGEON BR FRAGILE-X SYNDROME - SEARCH FOR PHENOTYPIC MANIFESTATIONS AT LOCI FOR HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE AND GLUCOSE-6-PHOSPHATE-DEHYDROGENASE | 7 | 10 |
| 1323 | 5 | 27 | 1505 1996 NUCLEIC ACIDS RESEARCH 24(4):784-792 Mariappan SVS; Catasti P; Chen X; Ratliff R; Moyzis RK; Bradbury EM; Gupta G Solution structures of the individual single strands of the fragile X DNA triplets (GCC)(n)center dot(GGC)(n) | 10 | 48 |
| 1324 | 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 |
| 1325 | 10 | 16 | 1582 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(3):161-166 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; Naeem R A five-year experience with fragile X testing - Setting laboratory standards of practice and a cost-effective protocol | 1 | 2 |
| 1326 | 1 | 1 | 1583 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(5):304-304 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; Naeem R Five-year experience with Fragile X-testing - Setting laboratory standards of practice and a cost-effective protocol (vol 6, pg 161, 1997) | 0 | 0 |
| 1327 | 0 | 0 | 1270 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):671-671 MARINI T; PFLUEGER S; NABER S; KARPELLS S; NAEEM R A 5-YEAR EXPERIENCE WITH FRAGILE-X TESTING | 0 | 0 |
| 1328 | 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 |
| 1329 | 1 | 2 | 1902 2000 HUMAN REPRODUCTION 15(8):1874-1875 Marozzi A Regarding recall bias in the association between idiopathic premature ovarian failure and fragile X premutation | 0 | 0 |
| 1330 | 16 | 41 | 1900 2000 HUMAN REPRODUCTION 15(1):197-202 Marozzi A; Vegetti W; Manfredini E; Tibiletti MG; Testa G; Crosignani PG; Ginelli E; Meneveri R; Dalpra L Association between idiopathic premature ovarian failure and fragile X premutation | 10 | 29 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1331 | 9 | 16 | 2314 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 124A(2):213-215 Marshall I; Betensky BP; Goseco A; Vogiatzi MV; Flieder D Fragile x and mosaic 45,X/46,XY mixed gonadal dysgenesis in a girl with ambiguous genitalia | 0 | 0 |
| 1332 | 3 | 11 | 1555 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 69(1):114-116 Martin NG; Healey SC; Pangan TS; Heath AC; Turner G Do mothers of dizygotic twins have earlier menopause? A role for fragile X? | 5 | 12 |
| 1333 | 15 | 22 | 968 1992 CLINICAL GENETICS 42(1):22-26 MARTINEZ F; BADIA L; PRIETO F A FRAGILE-X FAMILY WITH HIGH PENETRANCE IN FEMALES - RISK HETEROGENEITY | 0 | 2 |
| 1334 | 0 | 0 | 1841 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):236-236 Mathews DJ; Hudson R; Eichier E; Chakravarti A Sequence variation and linkage disequilibrium at the fragile X syndrome locus. | 0 | 0 |
| 1335 | 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 |
| 1336 | 0 | 0 | 488 1987 PEDIATRIC NEUROLOGY 3(5):284-287 MATSUISHI T; SHIOTSUKI Y; NIIKAWA N; KATAFUCHI Y; OTAKI E; ANDO H; YAMASHITA Y; HORIKAWA M; URABE F; KURIYA N; YAMASHITA F FRAGILE-X SYNDROME IN JAPANESE PATIENTS WITH INFANTILE-AUTISM | 4 | 6 |
| 1337 | 16 | 81 | 50 1982 ARCHIVES FRANCAISES DE PEDIATRIE 39(8):633-639 MATTEI JF FRAGILE X-LINKED MENTAL-RETARDATION | 3 | 3 |
| 1338 | 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 |
| 1339 | 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 |
| 1340 | 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 |
| 1341 | 0 | 0 | 269 1985 CLINICAL GENETICS 28(5):449-449 MAVROU A; SYRROU M; TSENGHI C; AGELAKIS M; YOUROUKOS S; METAXOTOU C FRAGILE X-SYNDROME AND MENTAL-RETARDATION IN GREECE | 0 | 0 |
| 1342 | 8 | 13 | 554 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):735-739 MAVROU A; SYRROU M; TSENGHI C; AGELAKIS M; YOUROUKOS S; METAXOTOU C MARTIN-BELL SYNDROME IN GREECE, WITH REPORT OF ANOTHER 47,XXY FRAGILE X PATIENT | 7 | 10 |
| 1343 | 0 | 0 | 2160 2002 LANCET NEUROLOGY 1(3):141-141 May TS Evidence of altered synaptic plasticity found in fragile X syndrome | 0 | 0 |
| 1344 | 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 |
| 1345 | 38 | 52 | 2272 2003 HUMAN MOLECULAR GENETICS 12(23):3087-3096 Mazroui R; Huot ME; Tremblay S; Boilard N; Labelle Y; Khandjian EW Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs | 2 | 2 |
| 1346 | 26 | 57 | 2145 2002 HUMAN MOLECULAR GENETICS 11(24):3007-3017 Mazroui R; Huot ME; Tremblay S; Filion C; Labelle Y; Khandjian EW Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression | 10 | 18 |
| 1347 | 57 | 117 | 1945 2000 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 6(2):96-106 Mazzocco MMM Advances in research on the fragile X syndrome | 18 | 20 |
| 1348 | 11 | 91 | 2035 2001 JOURNAL OF LEARNING DISABILITIES 34(6):520-533 Mazzocco MMM Math learning disability and math LD subtypes: Evidence from studies of Turner syndrome, fragile X syndrome, and neurofibromatosis type 1 | 2 | 7 |
| 1349 | 12 | 36 | 1674 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(6):509-517 Mazzocco MMM; Baumgardner T; Freund LS; Reiss AL Social functioning among girls with fragile X or Turner syndrome and their sisters | 8 | 11 |
| 1350 | 27 | 61 | 1382 1995 NEUROPSYCHOLOGY 9(4):470-480 MAZZOCCO MMM; FREUND LS; BAUMGARDNER TL; FORMAN L; REISS AL NEUROPSYCHOLOGICAL AND PSYCHOSOCIAL EFFECTS OF THE FMR-1 FULL MUTATION - CASE-REPORT OF MONOZYGOTIC TWINS DISCORDANT FOR THE FRAGILE-X SYNDROME | 5 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1351 | 10 | 30 | 997 1992 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 31(6):1141-1148 MAZZOCCO MMM; HAGERMAN RJ; CRONISTERSILVERMAN A; PENNINGTON BF SPECIFIC FRONTAL-LOBE DEFICITS AMONG WOMEN WITH THE FRAGILE-X GENE | 46 | 61 |
| 1352 | 1 | 14 | 914 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):78-86 MAZZOCCO MMM; HAGERMAN RJ; PENNINGTON BF PROBLEM-SOLVING LIMITATIONS AMONG CYTOGENETICALLY EXPRESSING FRAGILE-X WOMEN | 23 | 31 |
| 1353 | 12 | 31 | 1431 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):323-328 Mazzocco MMM; Holden JJA Neuropsychological profiles of three sisters homozygous for the fragile X premutation | 5 | 7 |
| 1354 | 24 | 61 | 1599 1997 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 27(4):415-435 Mazzocco MMM; Kates WR; Baumgardner TL; Freund LS; Reiss AL Autistic behaviors among girls with fragile X syndrome | 19 | 24 |
| 1355 | 7 | 18 | 1342 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):396-404 Mazzocco MMM; Lachiewicz AM; Kovar CG; Freund LS; Baumgardner TL; Dykens E Psychological and emotional studies of the fragile X mutation - A workshop summary | 0 | 0 |
| 1356 | 3 | 22 | 1149 1993 YOUNG CHILDREN 49(1):73-77 MAZZOCCO MMM; OCONNOR R FRAGILE-X SYNDROME - A GUIDE FOR TEACHERS OF YOUNG-CHILDREN | 0 | 1 |
| 1357 | 14 | 37 | 1110 1993 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 14(5):328-335 MAZZOCCO MMM; PENNINGTON BF; HAGERMAN RJ THE NEUROCOGNITIVE PHENOTYPE OF FEMALE CARRIERS OF FRAGILE-X - ADDITIONAL EVIDENCE FOR SPECIFICITY | 68 | 87 |
| 1358 | 10 | 23 | 1230 1994 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 24(4):473-485 MAZZOCCO MMM; PENNINGTON BF; HAGERMAN RJ SOCIAL COGNITION SKILLS AMONG FEMALES WITH FRAGILE-X | 9 | 12 |
| 1359 | 10 | 39 | 1671 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(4):321-328 Mazzocco MMM; Pulsifer M; Fiumara A; Cocuzza M; Nigro F; Incorpora G; Barone R Brief report: Autistic behaviors among children with fragile X or Rett syndrome: Implications for the classification of pervasive developmental disorder | 4 | 8 |
| 1360 | 0 | 0 | 1032 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):143-143 MAZZOCCO MMM; WHITE BN; HOLDEN JJA THE FRAGILE X SYNDROME - A FAMILY WITH 3 HOMOZYGOUS FRA(X) SISTERS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1361 | 0 | 0 | 770 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):303-303 MCCOMBS J; ROUSE B; LOCKHART L; HOWARDPEEBLES P PRENATAL IDENTIFICATION OF FRAGILE-X AND A MARKER CHROMOSOME | 0 | 0 |
| 1362 | 5 | 20 | 1721 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 82(3):206-211 McConkie-Rosell A; Spiridigliozzi GA; Rounds K; Dawson DV; Sullivan JA; Burgess D; Lachiewicz AM Parental attitudes regarding carrier testing in children at risk for fragile X syndrome | 2 | 7 |
| 1363 | 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 |
| 1364 | 6 | 26 | 1982 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 98(1):37-45 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Longitudinal study of the carrier testing process for fragile X syndrome: Perceptions and coping | 2 | 3 |
| 1365 | 12 | 32 | 2097 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 110(1):36-44 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Carrier testing in fragile X syndrome: When to tell and test | 0 | 0 |
| 1366 | 23 | 41 | 1056 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(4):800-809 MCCONKIEROSELL A; LACHIEWICZ AM; SPIRIDIGLIOZZI GA; TARLETON J; SCHOENWALD S; PHELAN MC; GOONEWARDENA P; DING XH; BROWN WT EVIDENCE THAT METHYLATION OF THE FMR-I LOCUS IS RESPONSIBLE FOR VARIABLE PHENOTYPIC-EXPRESSION OF THE FRAGILE-X SYNDROME | 63 | 99 |
| 1367 | 0 | 0 | 1341 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):390-395 McConkieRosell A; Robinson H; Wake S; Staley L; Heller K; Cronister A Educating extended family members about the inheritance of the fragile X syndrome | 0 | 1 |
| 1368 | 14 | 21 | 1297 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 59(4):426-430 MCCONKIEROSELL A; ROBINSON H; WAKE S; STALEY LW; HELLER K; CRONISTER A DISSEMINATION OF GENETIC RISK INFORMATION TO RELATIVES IN THE FRAGILE-X SYNDROME - GUIDELINES FOR GENETIC COUNSELORS | 6 | 7 |
| 1369 | 8 | 29 | 1553 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 68(1):62-69 McConkieRosell A; Spiridigliozzi GA; Iafolla T; Tarleton J; Lachiewicz AM Carrier testing in the fragile X syndrome: Attitudes and opinions of obligate carriers | 7 | 13 |
| 1370 | 0 | 0 | 117 1983 CLINICAL GENETICS 23(3):216-216 MCDERMOTT A MORE ON THE FRAGILE-X, WITH PARTICULAR REFERENCE TO FIBROBLAST AND AMNIOTIC-FLUID CULTURE, AND X-INACTIVATION | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1371 | 8 | 31 | 143 1983 JOURNAL OF MEDICAL GENETICS 20(3):169-178 MCDERMOTT A; WALTERS R; HOWELL RT; GARDNER A FRAGILE X-CHROMOSOME - CLINICAL AND CYTOGENETIC STUDIES ON CASES FROM 7 FAMILIES | 13 | 18 |
| 1372 | 8 | 25 | 333 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):353-358 MCGILLIVRAY BC; HERBST DS; DILL FJ; SANDERCOCK HJ; TISCHLER B INFANTILE-AUTISM - AN OCCASIONAL MANIFESTATION OF FRAGILE-(X) MENTAL-RETARDATION | 19 | 28 |
| 1373 | 0 | 1 | 1471 1996 CONTEMPORARY PSYCHOLOGY 41(5):488-489 McGraw KO Behavior and development in fragile X syndrome - Dykens,EM, Hodapp,RM, Leckman,JF | 0 | 0 |
| 1374 | 0 | 0 | 2136 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:232-232 McKelvie KB; Reynolds A; Tassone F; Taylor AK; Hagerman RJ Evidence for skewed X chromosome inactivation in females with the fragile X full mutation | 0 | 0 |
| 1375 | 0 | 0 | 604 1988 JOURNAL OF MEDICAL GENETICS 25(2):131-131 MCKINLEY MJ; KEARNEY LU; NICOLAIDES K PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY PLACENTAL BIOPSY | 0 | 0 |
| 1376 | 21 | 61 | 527 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):355-368 MCKINLEY MJ; KEARNEY LU; NICOLAIDES KH; GOSDEN CM; WEBB TP; FRYNS JP PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME BY PLACENTAL (CHORIONIC VILLI) BIOPSY CULTURE | 8 | 13 |
| 1377 | 1 | 4 | 432 1987 BRITISH MEDICAL JOURNAL 295(6603):922-922 MCKINLEY MJ; NICOLAIDES KH; KEARNEY LU; HERON O FRAGILE-X SYNDROME | 1 | 3 |
| 1378 | 15 | 25 | 1446 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):428-433 Meadows KL; Pettay D; Newman J; Hersey J; Ashley AE; Sherman SL Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population | 9 | 25 |
| 1379 | 27 | 77 | 1514 1996 SCREENING 4(4):175-192 Meadows KL; Sherman SL Fragile X syndrome: Examination of issues pertaining to population-based screening | 2 | 2 |
| 1380 | 0 | 0 | 2207 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):314-314 Medne L; Russell K; Ming J; Krantz ID; Souders M; Levy S; Gupta A; Spinner NB; Zackai EH; Morrissette JJD Subtelomeric FISH analysis in 108 autistic patients as adjunct to chromosome analysis and fragile X testing | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1381 | 3 | 53 | 2368 2004 QUALITATIVE HEALTH RESEARCH 14(6):741-759 Medved MI; Brockmeier J Making sense of traumatic experiences: Telling your life with fragile X syndrome | 0 | 0 |
| 1382 | 21 | 33 | 1220 1994 HUMAN MOLECULAR GENETICS 3(4):615-620 MEIJER H; DEGRAAFF E; MERCKX DML; JONGBLOED RJE; DEDIESMULDERS CEM; ENGELEN JJM; FRYNS JP; CURFS PMG; OOSTRA BA A DELETION OF 1.6 KB PROXIMAL TO THE CGG REPEAT OF THE FMR1 GENE CAUSES THE CLINICAL PHENOTYPE OF THE FRAGILE X SYNDROME | 46 | 78 |
| 1383 | 1 | 2 | 681 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(3):433-433 MEISNER LF FRAGILE-X FREQUENCY | 0 | 0 |
| 1384 | 13 | 21 | 1786 1999 GENETIC TESTING 3(3):301-304 Melis MA; Addis M; Lepiani C; Congeddu E; Cossu P; Cao A A strategy for fragile-X carrier screening | 0 | 2 |
| 1385 | 5 | 13 | 836 1991 BIOLOGICAL PSYCHIATRY 29(3):298-299 MENDLEWICZ J; HIRSCH D BIPOLAR MANIC-DEPRESSIVE ILLNESS AND THE FRAGILE-X SYNDROME | 0 | 1 |
| 1386 | 14 | 57 | 2367 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(10):3615-3620 Menon V; Leroux J; White CD; Reiss AL Frontostriatal deficits in fragile X syndrome: Relation to FMR1 gene expression | 0 | 0 |
| 1387 | 15 | 18 | 1244 1994 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 33(9):1316-1321 MERENSTEIN SA; SHYU V; SOBESKY WE; STALEY L; BERRYKRAVIS E; NELSON DL; LUGENBEEL KA; TAYLOR AK; PENNINGTON BF; HAGERMAN RJ FRAGILE-X SYNDROME IN A NORMAL IQ MALE WITH LEARNING AND EMOTIONAL-PROBLEMS | 18 | 22 |
| 1388 | 0 | 0 | 1490 1996 JOURNAL OF INVESTIGATIVE MEDICINE 44(1):A119-A119 Merenstein SA; Sobesky WE; Taylor AK; Tran HX; Riddle JE; Hagerman RJ Molecular clinical correlations in males with fragile X syndrome. | 0 | 0 |
| 1389 | 0 | 0 | 1907 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :57-57 Merin NM; Menon V; White CD; Glover GH; Reiss AL Gaze processing deficits in fragile X syndrome investigated using fMRI | 0 | 0 |
| 1390 | 2 | 31 | 629 1989 CLINICAL GENETICS 36(1):15-24 MERYASH DL PERCEPTION OF BURDEN AMONG AT-RISK WOMEN OF RAISING A CHILD WITH FRAGILE-X SYNDROME | 2 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1391 | 0 | 0 | 658 1989 PEDIATRIC RESEARCH 25(4):A16-A16 MERYASH DL PERCEPTION OF BURDEN AMONG AT-RISK WOMEN OF RAISING A CHILD WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1392 | 4 | 14 | 957 1992 AMERICAN JOURNAL ON MENTAL RETARDATION 96(5):528-535 MERYASH DL CHARACTERISTICS OF FRAGILE-X RELATIVES WITH DIFFERENT ATTITUDES TOWARD TERMINATING AN AFFECTED PREGNANCY | 4 | 5 |
| 1393 | 1 | 13 | 571 1988 CLINICAL GENETICS 33(5):349-355 MERYASH DL; ABUELO D COUNSELING NEEDS AND ATTITUDES TOWARD PRENATAL-DIAGNOSIS AND ABORTION IN FRAGILE-X FAMILIES | 5 | 17 |
| 1394 | 2 | 16 | 172 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):159-174 MERYASH DL; CRONK CE; SACHS B; GERALD PS AN ANTHROPOMETRIC STUDY OF MALES WITH THE FRAGILE-X SYNDROME | 26 | 43 |
| 1395 | 0 | 29 | 68 1982 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 12(3):295-301 MERYASH DL; SZYMANSKI LS; GERALD PS INFANTILE-AUTISM ASSOCIATED WITH THE FRAGILE-X SYNDROME | 44 | 71 |
| 1396 | 20 | 36 | 1690 1998 JOURNAL OF PEDIATRICS 133(3):363-365 Meyer GA; Blum NJ; Hitchcock W; Fortina P Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorder | 0 | 3 |
| 1397 | 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 |
| 1398 | 12 | 39 | 1558 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 74(2):167-171 Miezejeski CM; Heaney G; Belser R; Brown WT; Jenkins EC; Sersen EA Longer brainstem auditory evoked response latencies of individuals with fragile X syndrome related to sedation | 0 | 0 |
| 1399 | 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 |
| 1400 | 4 | 16 | 403 1986 NEUROPSYCHOLOGIA 24(3):405-409 MIEZEJESKI CM; JENKINS EC; HILL AL; WISNIEWSKI K; FRENCH JH; BROWN WT A PROFILE OF COGNITIVE DEFICIT IN FEMALES FROM FRAGILE-X FAMILIES | 47 | 60 |
Page 14: 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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