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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 15: 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 |
|---|---|---|---|---|---|
| 1401 | 14 | 40 | 939 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):291-298 MIGEON BR CONCERNING THE ROLE OF X-INACTIVATION AND DNA METHYLATION IN FRAGILE X-SYNDROME | 3 | 4 |
| 1402 | 1 | 11 | 1062 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 46(6):685-686 MIGEON BR ROLE OF DNA METHYLATION IN X-INACTIVATION AND THE FRAGILE X-SYNDROME | 2 | 3 |
| 1403 | 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 |
| 1404 | 0 | 0 | 1278 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1273-1273 MILA M; CASTELLVIBEL S; BARCELO A; SANCHEZ A; JIMENEZ D; MANDEL JL; ESTIVILL X MUTATIONS IN THE CPG ISLAND OF THE FMR1 GENE - ARE THEY RESPONSIBLE FOR FRAGILE-X SYNDROME | 0 | 0 |
| 1405 | 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 |
| 1406 | 21 | 34 | 1216 1994 HUMAN GENETICS 94(4):395-400 MILA M; KRUYER H; GLOVER G; SANCHEZ A; CARBONELL P; CASTELLVIBEL S; VOLPINI V; ROSELL J; GABARRON J; LOPEZ I; VILLA M; BALLESTA F; ESTIVILL X MOLECULAR ANALYSIS OF THE (CGG)(N) EXPANSION IN THE FMR-1 GENE IN 59 SPANISH FRAGILE-X SYNDROME FAMILIES | 12 | 16 |
| 1407 | 8 | 25 | 2060 2001 REVISTA DE NEUROLOGIA 33:S20-S23 Mila M; Mallolas J Fragile X syndrome: Premature ovarian failure. Preimplantation and preconception genetic diagnosis | 0 | 0 |
| 1408 | 15 | 19 | 1393 1996 ACTA BIOCHIMICA POLONICA 43(2):383-388 Milewski M; Zygulska M; Bal J; Deelen WH; Obersztyn E; Bocian E; Halley DJJ; Horst J; Mazurczak T Analysis of unstable DNA sequence in FRM1 gene in Polish families with fragile X syndrome | 0 | 0 |
| 1409 | 8 | 12 | 1774 1999 CLINICAL GENETICS 56(1):98-99 Millan JM; Martinez F; Cadroy A; Gandia J; Casquero M; Beneyto M; Badin L; Prieto F Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain | 2 | 3 |
| 1410 | 0 | 0 | 1684 1998 JOURNAL OF INVESTIGATIVE MEDICINE 46(1):87A-87A Miller LJ; McIntosh D; McGrath J; Shyu V; Lampe M; Taylor AK; Tassone F; Neitzel K; Stackhouse T; Hagerman RJ Electrodermal responses to sensory stimuli in individuals with fragile X sydrome. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1411 | 16 | 54 | 1727 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):268-279 Miller LJ; McIntosh DN; McGrath J; Shyu V; Lampe M; Taylor AK; Tassone F; Neitzel K; Stackhouse T; Hagerman RJ Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: A preliminary report | 29 | 36 |
| 1412 | 0 | 18 | 1886 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12(1):381-384 Miller WJ; Skinner JA; Foss GS; Davies KE Localization of the fragile X mental retardation 2 (FMR2) protein in mammalian brain | 0 | 7 |
| 1413 | 6 | 11 | 518 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):177-183 MILONE G; CONTI L; RIZZO R; SANFILIPPO S; SAMMITO V; ROMANO C A DERMATOGLYPHIC STUDY OF A GROUP OF SICILIAN CHILDREN WITH FRAGILE-X SYNDROME | 1 | 2 |
| 1414 | 1 | 5 | 253 1985 AMERICAN JOURNAL OF PUBLIC HEALTH 75(7):715-716 MILUNSKY A AN IMPORTANT CLINICAL APPROACH IN DETECTING THE FRAGILE X-SYNDROME | 0 | 1 |
| 1415 | 13 | 25 | 1060 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 45(5):589-593 MILUNSKY A; HUANG XL; AMOS JA; HERSKOWITZ J; FARRER LA; WYANDT HE 46,XY/47,XYY MALE WITH THE FRAGILE X-SYNDROME - CYTOGENETIC AND MOLECULAR STUDIES | 3 | 4 |
| 1416 | 3 | 5 | 2315 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 125A(3):320-320 Milunsky JM; Maher TA Fragile X carrier screening and spinocerebellar ataxia in older males | 0 | 0 |
| 1417 | 20 | 26 | 1747 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):204-207 Mingroni-Netto RC; Costa SS; Angeli CB; Vianna-Morgante AM DXS548/FRAXAC1 haplotypes in fragile X chromosomes in the Brazilian population | 0 | 3 |
| 1418 | 25 | 35 | 1571 1997 BRAZILIAN JOURNAL OF GENETICS 20(4):731-739 Mingroni-Netto RC; Pavanello RCM; Otto PA; Vianna-Morgante AM Experience with molecular and cytogenetic diagnosis of fragile X syndrome in Brazilian families | 2 | 2 |
| 1419 | 1 | 1 | 682 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(3):434-434 MINGRONINETTO RC; ROSENBERG C; VIANNAMORGANTE AM; PAVANELLO RCM FRAGILE-X FREQUENCY - RESPONSE | 0 | 0 |
| 1420 | 19 | 43 | 677 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 35(1):22-27 MINGRONINETTO RC; ROSENBERG C; VIANNAMORGANTE AM; PAVANELLO RDM FRAGILE-X FREQUENCY IN A MENTALLY-RETARDED POPULATION IN BRAZIL | 5 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1421 | 0 | 0 | 2215 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):457-457 Mirakhory M; Aleyassin A Study of folic acid pathway genes alteration in fragile X syndrome. | 0 | 0 |
| 1422 | 6 | 36 | 2336 2004 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 25(1):21-27 Mirrett PL; Bailey DB; Roberts JE; Hatton DD Developmental screening and detection of developmental delays in infants and toddlers with fragile X syndrome | 0 | 0 |
| 1423 | 23 | 69 | 2291 2003 LANGUAGE SPEECH AND HEARING SERVICES IN SCHOOLS 34(4):320-331 Mirrett PL; Roberts JE Early intervention practices and communication intervention strategies for young males with fragile X syndrome | 0 | 0 |
| 1424 | 0 | 0 | 2287 2003 JOURNAL OF PSYCHOSOMATIC RESEARCH 55(2):156-156 Mirzaei M; Karam GA; Mahmoudi M Evaluation of prevalence the fragile X syndrome in 52 patients with moderate mental retardation with cytogenetic methods. | 0 | 0 |
| 1425 | 3 | 11 | 1860 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(4):358-360 Missirian C; Moncla A; Voelckel MA; Ravix V; Philip N Fragile X syndrome and 22q11.2 microdeletion in the same sibship | 0 | 0 |
| 1426 | 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 |
| 1427 | 11 | 34 | 1385 1995 NUCLEIC ACIDS RESEARCH 23(11):1876-1881 MITCHELL JE; NEWBURY SF; MCCLELLAN JA COMPACT STRUCTURES OF D(CNG)(N) OLIGONUCLEOTIDES IN SOLUTION AND THEIR POSSIBLE RELEVANCE TO FRAGILE-X AND RELATED HUMAN GENETIC-DISEASES | 2 | 31 |
| 1428 | 0 | 0 | 56 1982 CLINICAL RESEARCH 30(5):A891-A891 MIXON C; DEV V EFFECT OF FUDR AND METHIONINE ON THE EXPRESSION OF FRAGILE X IN A LYMPHOBLASTOID CELL-LINE | 1 | 1 |
| 1429 | 0 | 2 | 98 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A144-A144 MIXON C; DEV VG INHIBITION OF FRAGILE-X EXPRESSION BY 5-AZACYTIDINE (AZA) AND BY S-ADENOSYLHOMOCYSTEINE (SAH) | 0 | 0 |
| 1430 | 0 | 0 | 166 1984 ALABAMA JOURNAL OF MEDICAL SCIENCES 21(3):322-322 MIXON JC INHIBITION OF FRAGILE-X EXPRESSION BY 5-AZACYTIDINE (AZA) AND BY S-ADENOSYLHOMOCYSTEINE (SAH) | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1431 | 2 | 13 | 104 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):1270-1275 MIXON JC; DEV VG FRAGILE-X EXPRESSION IS DECREASED BY 5-AZACYTIDINE AND S-ADENOSYLHOMOCYSTEINE | 4 | 9 |
| 1432 | 5 | 15 | 165 1984 ALABAMA JOURNAL OF MEDICAL SCIENCES 21(3):284-286 MIXON JC; DEV VG UNDERSTANDING THE FRAGILE X-SYNDROME | 0 | 2 |
| 1433 | 0 | 1 | 384 1986 FEDERATION PROCEEDINGS 45(3):702-702 MIXON JC; DEV VG DIMETHYLSULFOXIDE (DMSO) INCREASES FRAGILE X EXPRESSION IN THE PRESENCE OF 5-FLUORO-2'-DEOXYURIDINE (FUDR) | 0 | 0 |
| 1434 | 0 | 0 | 436 1987 CLINICAL RESEARCH 35(1):A60-A60 MIXON JC; DEV VG DIMETHYLSULFOXIDE (DMSO) INCREASES FRAGILE-X (FRA-X) EXPRESSION IN THE PRESENCE OF 5-FLOURO-2'-DEOXYURIDINE (FDUMP) | 0 | 0 |
| 1435 | 10 | 13 | 2074 2001 SCIENCE 294(5551):2487-2488 Moine H; Mandel JL Biomedicine - Do G quartets orchestrate fragile X pathology? | 3 | 8 |
| 1436 | 1 | 26 | 2244 2003 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 303(1):81-90 Monleon D; Esteve V; Celda B NMR study of hexanucleotide d(CCGCGG)(2) containing two triplet repeats of fragile X syndrome | 0 | 0 |
| 1437 | 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 |
| 1438 | 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 |
| 1439 | 1 | 1 | 1990 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 105(7):585-585 Moore CJ; Daly E; Tassone F; Jacobs PA; Davies KE; Murphy KC; Murphy KGM Neuroanatomical effect of FMR1 gene mRNA in premutation carriers of Fragile X syndrome | 0 | 0 |
| 1440 | 0 | 0 | 2046 2001 NEUROIMAGE 13(6):S1076-S1076 Moore CJ; Daly EM; Schmitz N; Murphy KC; Murphy DGM Premutation expansion of CGG triplet repeats affects brain; a study of male carriers of Fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1441 | 5 | 11 | 966 1992 BRITISH MEDICAL JOURNAL 305(6847):208-208 MOORE DWY NEW DEVELOPMENTS IN THE FRAGILE-X SYNDROME | 1 | 1 |
| 1442 | 3 | 4 | 1128 1993 LANCET 342(8886-7):1563-1564 MOORE DY DIAGNOSING FRAGILE X-SYNDROME | 0 | 0 |
| 1443 | 6 | 17 | 680 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(2):265-267 MOORE PSJ; CHUDLEY AE; WINTER JSD TRUE PRECOCIOUS PUBERTY IN A GIRL WITH THE FRAGILE X-SYNDROME | 10 | 13 |
| 1444 | 5 | 15 | 826 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 39(3):374-375 MOORE PSJ; CHUDLEY AE; WINTER JSD PITUITARY-GONADAL AXIS IN PREPUBERTAL BOYS WITH THE FRAGILE-X SYNDROME | 5 | 7 |
| 1445 | 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 |
| 1446 | 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 |
| 1447 | 20 | 52 | 2185 2002 NEURON 34(6):961-972 Morales J; Hiesinger PR; Schroeder AJ; Kume K; Verstreken P; Jackson FR; Nelson DL; Hassan BA Drosophila fragile X protein, DFXR, regulates neuronal morphology and function in the brain | 17 | 25 |
| 1448 | 0 | 1 | 148 1983 JOURNAL OF MEDICAL GENETICS 20(6):476-476 MORICPETROVIC S; LACA Z A FATHER AND DAUGHTER WITH FRAGILE X-CHROMOSOME | 5 | 7 |
| 1449 | 0 | 0 | 1566 1997 ARCHIVES DE PEDIATRIE 4(2):195-195 Mornet E Fragile X syndrome - Response | 0 | 0 |
| 1450 | 11 | 29 | 1095 1993 HUMAN GENETICS 92(4):373-378 MORNET E; BOGYO A; DELUCHAT C; SIMONBOUY B; MATHIEU M; THEPOT F; GRISARD MC; LEGUERN E; BOUE J; BOUE A MOLECULAR ANALYSIS OF A RING CHROMOSOME-X IN A FAMILY WITH FRAGILE-X SYNDROME | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1451 | 8 | 10 | 1643 1998 CLINICAL GENETICS 53(3):200-201 Mornet E; Chateau C; Simon-Bouy B; Serre JL The intermediate alleles of the fragile X CGG repeat in patients with mental retardation | 3 | 6 |
| 1452 | 17 | 26 | 1481 1996 HUMAN GENETICS 97(4):512-515 Mornet E; Chateau C; Taillandier A; SimonBouy B; Serre JL Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndrome | 4 | 8 |
| 1453 | 7 | 7 | 1078 1993 CLINICAL GENETICS 43(3):157-159 MORNET E; JOKIC M; BOGYO A; TEJADA I; DELUCHAT C; BOUE J; BOUE A AFFECTED SIBS WITH FRAGILE-X SYNDROME EXHIBIT AN AGE-DEPENDENT DECREASE IN THE SIZE OF THE FRAGILE-X FULL MUTATION | 5 | 8 |
| 1454 | 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 |
| 1455 | 2 | 6 | 1311 1995 BONE MARROW TRANSPLANTATION 16(4):625-626 MORTON J; ARNOLD L; FLETCHER B; MCCARTHY C; ROWELL J; DURRANT S ALLOGENEIC BMT FROM A DONOR WITH FRAGILE-X SYNDROME - CYTOGENETIC AND MOLECULAR EVALUATION | 0 | 0 |
| 1456 | 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 |
| 1457 | 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 |
| 1458 | 7 | 17 | 1014 1992 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 89(9):4215-4217 MORTON NE; MACPHERSON JN POPULATION-GENETICS OF THE FRAGILE-X SYNDROME - MULTIALLELIC MODEL FOR THE FMR1 LOCUS | 47 | 78 |
| 1459 | 0 | 0 | 1622 1997 NEUROLOGY 48(3):5062-5062 Mostofsky SH; Mazzocco MM; Aakalu G; Warsofsky IS; Denckla MB; Reiss AL Aberrant posterior vermis size in fragile X syndrome: Correlation with neurocognitive performance | 0 | 0 |
| 1460 | 18 | 63 | 1693 1998 NEUROLOGY 50(1):121-130 Mostofsky SH; Mazzocco MMM; Aakalu G; Warsofsky IS; Denckla MB; Reiss AL Decreased cerebellar posterior vermis size in fragile X syndrome - Correlation with neurocognitive performance | 18 | 44 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1461 | 0 | 0 | 1694 1998 NEUROLOGY 50(4):A86-A86 Mostofsky SH; Reiss AL; Freund L Examination of posterior vermis size in young males with fragile X syndrome | 0 | 0 |
| 1462 | 21 | 35 | 1594 1997 HUMAN MOLECULAR GENETICS 6(7):971-979 Moutou C; Vincent MC; Biancalana V; Mandel JL Transition from premutation to full mutation in fragile X syndrome is likely to be prezygotic | 18 | 33 |
| 1463 | 18 | 19 | 1300 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(4):302-306 MUELLER OT; HARTSFIELD JK; AMAR MJA; GALLARDO LA; KOUSSEFF BG FRAGILE-X SYNDROME - DISCORDANT LEVELS OF CGG REPEAT MOSAICISM IN 2 BROTHERS | 2 | 5 |
| 1464 | 0 | 0 | 1046 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1206-1206 MUELLER OT; HARTSFIELD JK; GALLARDO LA; KOUSSEFF BG FRAGILE X-SYNDROME - DISCORDANT EXPRESSION OF FMR-1 WITH IDENTICAL SMALL CGG INSERTS IN 2 BROTHERS | 0 | 0 |
| 1465 | 5 | 13 | 541 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):567-580 MULLEY J; TURNER G; BAIN S; SUTHERLAND GR LINKAGE BETWEEN THE FRAGILE-X AND F9, DXS52 (ST14), DXS98 (4D-8) AND DXS105 (CX55.7) | 13 | 20 |
| 1466 | 7 | 20 | 417 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 27(2):435-448 MULLEY JC; GEDEON AK; THORN KA; BATES LJ; SUTHERLAND GR LINKAGE AND GENETIC-COUNSELING FOR THE FRAGILE-X USING DNA PROBE-52A, PROBE-F9, PROBE-DX13, AND PROBE-ST14 | 17 | 43 |
| 1467 | 5 | 13 | 415 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 26(4):987-990 MULLEY JC; SUTHERLAND GR FRAGILE-X TRANSMISSION AND THE DETERMINATION OF CARRIER PROBABILITIES FOR GENETIC-COUNSELING | 0 | 11 |
| 1468 | 0 | 0 | 366 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(4):352-352 MULLEY JC; THORN K; SUTHERLAND GR LINKAGE RELATIONSHIPS OF THE FRAGILE-X | 0 | 0 |
| 1469 | 14 | 20 | 991 1992 JOURNAL OF MEDICAL GENETICS 29(6):368-374 MULLEY JC; YU S; GEDEON AK; DONNELLY A; TURNER G; LOESCH D; CHAPMAN CJ; GARDNER RJM; RICHARDS RI; SUTHERLAND GR EXPERIENCE WITH DIRECT MOLECULAR DIAGNOSIS OF FRAGILE-X | 26 | 38 |
| 1470 | 8 | 29 | 240 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(3):463-472 MULLIGAN LM; PHILLIPS MA; FORSTERGIBSON CJ; BECKETT J; PARTINGTON MW; SIMPSON NE; HOLDEN JJA; WHITE BN GENETIC-MAPPING OF DNA SEGMENTS RELATIVE TO THE LOCUS FOR THE FRAGILE-X SYNDROME AT XQ27.3 | 6 | 49 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1471 | 1 | 1 | 976 1992 EUROPEAN JOURNAL OF PEDIATRICS 151(6):469-470 MUNDLOS S FRAGILE-X SOLVED | 0 | 0 |
| 1472 | 1 | 1 | 977 1992 EUROPEAN JOURNAL OF PEDIATRICS 151(8):617-617 MUNDLOS S GIRLS WITH THE FRAGILE-X SYNDROME | 0 | 0 |
| 1473 | 0 | 0 | 2183 2002 NEUROLOGY 58(7):A482-A482 Munhoz RP; Lozano AM; Lang AE Fragile X syndrome premutation mistaken as essential tremor: An unrecognized source of diagnostic confusion | 0 | 0 |
| 1474 | 0 | 0 | 1922 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:405-405 Munir F; Comish KM; Wilding J A neuropsychological profile of attention and hyperactivity in boys with fragile-X syndrome: Implications for clinical intervention | 0 | 0 |
| 1475 | 11 | 52 | 1874 2000 BRAIN AND COGNITION 44(3):387-401 Munir F; Cornish KM; Wilding J Nature of the working memory deficit in Fragile-X syndrome | 5 | 6 |
| 1476 | 13 | 47 | 1954 2000 NEUROPSYCHOLOGIA 38(9):1261-1270 Munir F; Cornish KM; Wilding J A neuropsychological profile of attention deficits in young males with fragile X syndrome | 13 | 15 |
| 1477 | 0 | 0 | 2180 2002 NEUROLOGY 58(6):987-987 Munoz DG Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X | 0 | 0 |
| 1478 | 20 | 43 | 1812 1999 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 38(10):1294-1301 Murphy DGM; Mentis MJ; Pietrini P; Grady CL; Moore CJ; Horwitz B; Hinton V; Dobkin CS; Schapiro MB; Rapoport SI Premutation female carriers of fragile X syndrome: A pilot study on brain anatomy and metabolism | 6 | 7 |
| 1479 | 0 | 0 | 1843 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):248-248 Murphy KM; Nunes ME Comparison of child-only versus mother/child sample collection in Fragile X testing. | 0 | 0 |
| 1480 | 45 | 118 | 2274 2003 INTERNATIONAL REVIEW OF RESEARCH IN MENTAL RETARDATION, VOL 27 27:83-119 Murphy MM; Abbeduto L Language and communication in fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1481 | 0 | 0 | 405 1986 PEDIATRIC RESEARCH 20(4):A269-A269 MURPHY PD; WATSON MS; KIDD KK; BREG WR MOLECULAR APPROACHES TO CARRIER DETECTION AND PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME (MCKUSICK NUMBER 30920) | 1 | 2 |
| 1482 | 2 | 9 | 790 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):305-310 MURPHY PD; WATSON MS; SHAPIRO LR; WILMOT PL; BREG WR DNA-BASED GENETIC TESTING IN 50 FRAGILE-X FAMILIES | 2 | 2 |
| 1483 | 11 | 12 | 929 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):181-186 MURPHY PD; WILMOT PL; SHAPIRO LR PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - RESULTS FROM PARALLEL MOLECULAR AND CYTOGENETIC STUDIES | 1 | 1 |
| 1484 | 0 | 0 | 1403 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):16-16 Murray A; Conway GS; Jacobs PA Premature ovarian failure and fragile X. | 0 | 0 |
| 1485 | 9 | 21 | 1884 2000 EUROPEAN JOURNAL OF HUMAN GENETICS 8(4):247-252 Murray A; Ennis S; MacSwiney F; Webb J; Morton NE Reproductive and menstrual history of females with fragile X expansions | 10 | 13 |
| 1486 | 2 | 4 | 1828 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):253-254 Murray A; Ennis S; Morton N No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers | 9 | 16 |
| 1487 | 9 | 25 | 2011 2001 COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING 4(3):265-272 Murray J; Cuckle H Cystic fibrosis and fragile X syndrome: The arguments for antenatal screening | 1 | 2 |
| 1488 | 0 | 1 | 760 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):270-270 MURTHY SK; KAR B FRAGILE-X SYNDROME IN MENTALLY-RETARDED POPULATION OF WESTERN INDIA | 0 | 0 |
| 1489 | 0 | 0 | 2232 2003 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 189(6):S117-S117 Musci TJ; Caughey AB Cost-effectiveness analysis of prenatal population-based fragile X carrier screening | 0 | 0 |
| 1490 | 7 | 34 | 1620 1997 NATURE STRUCTURAL BIOLOGY 4(9):712-716 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; Nilges M; Pastore A The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome | 5 | 40 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1491 | 1 | 1 | 1621 1997 NATURE STRUCTURAL BIOLOGY 4(10):840-840 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; Nilges M; Pastore A The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome (vol 4, pg 712, 1997) | 0 | 0 |
| 1492 | 9 | 43 | 1463 1996 CELL 85(2):237-245 Musco G; Stier G; Joseph C; Morelli MAC; Nilges M; Gibson TJ; Pastore A Three-dimensional structure and stability of the KH domain: Molecular insights into the fragile X syndrome | 20 | 167 |
| 1493 | 18 | 32 | 1883 2000 EPILEPSIA 41(1):19-23 Musumeci SA; Bosco P; Calabrese G; Bakker C; De Sarro GB; Elia M; Ferri R; Oostra BA Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome | 23 | 30 |
| 1494 | 9 | 28 | 580 1988 EPILEPSIA 29(1):41-47 MUSUMECI SA; COLOGNOLA RM; FERRI R; GIGLI GL; PETRELLA MA; SANFILIPPO S; BERGONZI P; TASSINARI CA FRAGILE-X SYNDROME - A PARTICULAR EPILEPTOGENIC EEG PATTERN | 17 | 38 |
| 1495 | 1 | 5 | 1224 1994 ITALIAN JOURNAL OF NEUROLOGICAL SCIENCES 15(7):365-368 MUSUMECI SA; ELIA M; FERRI R; SCUDERI C; DELGRACCO S EVOKED SPIKES AND GIANT SOMATOSENSORY-EVOKED POTENTIALS IN A PATIENT WITH FRAGILE-X SYNDROME | 3 | 8 |
| 1496 | 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 |
| 1497 | 3 | 10 | 825 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):511-513 MUSUMECI SA; FERRI R; ELIA M; COLOGNOLA RM; BERGONZI P; TASSINARI CA EPILEPSY AND FRAGILE-X SYNDROME - A FOLLOW-UP-STUDY | 21 | 36 |
| 1498 | 3 | 16 | 1326 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):218-222 Musumeci SA; Ferri R; Elia M; DalGracco S; Scuderi C; Stefanini MC; Castano A; Azan G Sleep neurophysiology in fragile X patients | 2 | 3 |
| 1499 | 1 | 4 | 1497 1996 JOURNAL OF SLEEP RESEARCH 5(4):272-272 Musumeci SA; Ferri R; Elia M; DelGracco S; Scuderi C; Stefanini MC Normal respiratory pattern during sleep in young fragile X-syndrome patients | 1 | 1 |
| 1500 | 22 | 54 | 1782 1999 EPILEPSIA 40(8):1092-1099 Musumeci SA; Hagerman RJ; Ferri R; Bosco P; Dalla Bernardina B; Tassinari CA; De Sarro GB; Elia M Epilepsy and EEG findings in males with fragile X syndrome | 9 | 18 |
Page 15: 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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