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Results: 1-25 | 26-50 | 51-71
Results: 26-50/71
TISSUE DIFFERENCES IN FRAGILE-X MOSAICS - MOSAICISM IN BLOOD-CELLS MAY DIFFER GREATLY FROM SKIN
Authors: DOBKIN CS NOLIN SL COHEN I SUDHALTER V BIALER MG DING XH JENKINS EC ZHONG N BROWN WT
Citation: Cs. Dobkin et al., TISSUE DIFFERENCES IN FRAGILE-X MOSAICS - MOSAICISM IN BLOOD-CELLS MAY DIFFER GREATLY FROM SKIN, American journal of medical genetics, 64(2), 1996, pp. 296-301
MOSAICISM FOR THE FMR1 GENE INFLUENCES ADAPTIVE SKILLS DEVELOPMENT INFRAGILE X-AFFECTED MALES
Authors: COHEN IL NOLIN SL SUDHALTER V DING XH DOBKIN CS BROWN WT
Citation: Il. Cohen et al., MOSAICISM FOR THE FMR1 GENE INFLUENCES ADAPTIVE SKILLS DEVELOPMENT INFRAGILE X-AFFECTED MALES, American journal of medical genetics, 64(2), 1996, pp. 365-369
A SURVEY OF FRAXE ALLELE SIZES IN 3 POPULATIONS
Authors: ZHONG N JU WN CURLEY D WANG DW PIETROFESA J WU GY SHEN Y PANG C POON P LIU XX GOU S KAJANOJA E RYYNANEN M DOBKIN C BROWN WT
Citation: N. Zhong et al., A SURVEY OF FRAXE ALLELE SIZES IN 3 POPULATIONS, American journal of medical genetics, 64(2), 1996, pp. 415-419
7TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X-LINKED AND X-LINKED MENTAL-RETARDATION
Authors: 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
Citation: L. Tranebjaerg et al., 7TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X-LINKED AND X-LINKED MENTAL-RETARDATION, American journal of medical genetics, 64(1), 1996, pp. 1-14
PRENATAL-DIAGNOSIS AND CARRIER SCREENING FOR FRAGILE-X BY PCR
Authors: BROWN WT NOLIN S HOUCK G DING XH GLICKSMAN A LI SY STARKHOUCK S BROPHY P DUNCAN C DOBKIN C JENKINS E
Citation: Wt. Brown et al., PRENATAL-DIAGNOSIS AND CARRIER SCREENING FOR FRAGILE-X BY PCR, American journal of medical genetics, 64(1), 1996, pp. 191-195
FRAGILE-X FOUNDER EFFECTS AND NEW MUTATIONS IN FINLAND
Authors: ZHONG N KAJANOJA E SMITS B PIETROFESA J CURLEY D WANG DW JU MN NOLIN S DOBKIN C RYYNANEN M BROWN WT
Citation: N. Zhong et al., FRAGILE-X FOUNDER EFFECTS AND NEW MUTATIONS IN FINLAND, American journal of medical genetics, 64(1), 1996, pp. 226-233
NO DETECTABLE MUTATIONS AT WERNER HELICASE LOCUS IN PROGERIA
Authors: OSHIMA J BROWN WT MARTIN GM
Citation: J. Oshima et al., NO DETECTABLE MUTATIONS AT WERNER HELICASE LOCUS IN PROGERIA, Lancet, 348(9034), 1996, pp. 1106-1106
FAMILIAL TRANSMISSION OF THE FMR1 CGG REPEAT
Authors: NOLIN SL LEWIS FA YE LL HOUCK GE GLICKSMAN AE LIMPRASERT P LI SY ZHONG N ASHLEY AE FEINGOLD E SHERMAN SL BROWN WT
Citation: Sl. Nolin et al., FAMILIAL TRANSMISSION OF THE FMR1 CGG REPEAT, American journal of human genetics, 59(6), 1996, pp. 1252-1261
THE MOLECULAR-BASIS OF FRAGILE SITES
Authors: DOBKIN C ZHONG N BROWN WT
Citation: C. Dobkin et al., THE MOLECULAR-BASIS OF FRAGILE SITES, American journal of human genetics, 59(2), 1996, pp. 478-478
TOWARD LOCALIZATION OF THE WERNER SYNDROME GENE BY LINKAGE DISEQUILIBRIUM AND ANCESTRAL HAPLOTYPING - LESSONS LEARNED FROM ANALYSIS OF 35 CHROMOSOME 8P11.1-21.1 MARKERS
Authors: GODDARD KAB YU CE OSHIMA J MIKI T NAKURA J PIUSSAN C MARTIN GM SCHELLENBERG GD WIJSMAN EM BROWN WT BURG G CERIMELE D COTTINI F EPSTEIN CJ FISCHER W FRACCARO M FUJIWARA Y FUKUCHI KI HIWADA K HOEHN H HOSOKAWA Y HURLIMANN AF ISHAWATA H KAMINO K KIHARA K KISO S LIN Y MAEDA T MATTHEWS J MATSUMURA T MCKAY JE MELARAGNO MI MITSUDA M MOTULSKY AG MURAKAMI T MURANO S NIIKAWA N POOT M OGIHARA T RIZZO M SAIDA T SCAPPATICCI S TANNOK TCA TAMAKI S UTSU N UYENO B WAKAYAMA A YANAGAWA M YEVICH II YOSHIDA S ZIGRANG W
Citation: Kab. Goddard et al., TOWARD LOCALIZATION OF THE WERNER SYNDROME GENE BY LINKAGE DISEQUILIBRIUM AND ANCESTRAL HAPLOTYPING - LESSONS LEARNED FROM ANALYSIS OF 35 CHROMOSOME 8P11.1-21.1 MARKERS, American journal of human genetics, 58(6), 1996, pp. 1286-1302
THE FRAXE SYNDROME - IS IT TIME FOR ROUTINE SCREENING
Authors: BROWN WT
Citation: Wt. Brown, THE FRAXE SYNDROME - IS IT TIME FOR ROUTINE SCREENING, American journal of human genetics, 58(5), 1996, pp. 903-905
POSITIVE FRAGILE-X MICROSATELLITE ASSOCIATIONS POINT TO A COMMON MECHANISM OF DYNAMIC MUTATION EVOLUTION
Authors: BROWN WT ZHONG N DOBKIN C
Citation: Wt. Brown et al., POSITIVE FRAGILE-X MICROSATELLITE ASSOCIATIONS POINT TO A COMMON MECHANISM OF DYNAMIC MUTATION EVOLUTION, American journal of human genetics, 58(3), 1996, pp. 641-643
COGNITIVE AND MOLECULAR ASPECTS OF FRAGILE-X
Authors: HINTON VJ HALPERIN JM DOBKIN CS DING XH BROWN WT MIEZEJESKI CM
Citation: Vj. Hinton et al., COGNITIVE AND MOLECULAR ASPECTS OF FRAGILE-X, Neuropsychology, development, and cognition. Section A, Journal of clinical and experimental neuropsychology, 17(4), 1995, pp. 518-528
PERSPECTIVES AND MOLECULAR DIAGNOSIS OF THE FRAGILE-X SYNDROME
Authors: BROWN WT
Citation: Wt. Brown, PERSPECTIVES AND MOLECULAR DIAGNOSIS OF THE FRAGILE-X SYNDROME, Clinics in laboratory medicine, 15(4), 1995, pp. 859
LACK OF SIGNIFICANT ASSOCIATION BETWEEN SPINA-BIFIDA AND THE FRAGILE-X SYNDROME
Authors: SCHIANO CM DEMB HB BROWN WT
Citation: Cm. Schiano et al., LACK OF SIGNIFICANT ASSOCIATION BETWEEN SPINA-BIFIDA AND THE FRAGILE-X SYNDROME, American journal of medical genetics, 59(4), 1995, pp. 526-526
FURTHER DELINEATION OF THE 14Q- SYNDROME - DOUBLE MOSAICISM OR CHIMERA IN A PROFOUNDLY MENTALLY-RETARDED INDIVIDUAL
Authors: YAO XL ADELMAN SA GENOVESE M WISNIEWSKI K BROWN WT JENKINS EC
Citation: Xl. Yao et al., FURTHER DELINEATION OF THE 14Q- SYNDROME - DOUBLE MOSAICISM OR CHIMERA IN A PROFOUNDLY MENTALLY-RETARDED INDIVIDUAL, American journal of human genetics, 57(4), 1995, pp. 586-586
DETERMINATION OF TRANSCRIPTION FACTORS BINDING TO THE FMR1 PROMOTER REGION
Authors: ZHONG N CURLEY D DOBKIN C BROWN WT
Citation: N. Zhong et al., DETERMINATION OF TRANSCRIPTION FACTORS BINDING TO THE FMR1 PROMOTER REGION, American journal of human genetics, 57(4), 1995, pp. 880-880
FRAGILE-X FOUNDER CHROMOSOME EFFECTS AND NEW MUTATIONS
Authors: BROWN WT ZHONG N KAJANOJA E SMITS B CURLEY D WANG D JU W HOUCK G NOLIN S RYYNANEN M
Citation: Wt. Brown et al., FRAGILE-X FOUNDER CHROMOSOME EFFECTS AND NEW MUTATIONS, American journal of human genetics, 57(4), 1995, pp. 913-913
EVIDENCE FOR A FAMILIAL FACTOR INVOLVED IN CGG REPEAT EXPANSION IN FRAGILE-X SYNDROME
Authors: NOLIN SL GLICKSMAN A LEWIS FA YE LL HOUCK GE ASHLEY AE SHERMAN SL BROWN WT
Citation: Sl. Nolin et al., EVIDENCE FOR A FAMILIAL FACTOR INVOLVED IN CGG REPEAT EXPANSION IN FRAGILE-X SYNDROME, American journal of human genetics, 57(4), 1995, pp. 965-965
NEW INTRAGENIC ALU POLYMORPHISMS IN THE FRAGILE-X GENE
Authors: CURLEY D ZHONG N WANG DW JU W DOBKIN C BROWN WT
Citation: D. Curley et al., NEW INTRAGENIC ALU POLYMORPHISMS IN THE FRAGILE-X GENE, American journal of human genetics, 57(4), 1995, pp. 1088-1088
DIFFERENCES BETWEEN MOSAICISM IN BLOOD-CELLS AND SKIN FIBROBLASTS SUGGEST THAT SHIN MAY BETTER PREDICT BRAIN-FUNCTION
Authors: DOBKIN CS NOLIN SL COHEN J SUDHALTER V BIALER MG DING XH JENKINS EC ZHONG N BROWN WT
Citation: Cs. Dobkin et al., DIFFERENCES BETWEEN MOSAICISM IN BLOOD-CELLS AND SKIN FIBROBLASTS SUGGEST THAT SHIN MAY BETTER PREDICT BRAIN-FUNCTION, American journal of human genetics, 57(4), 1995, pp. 1953-1953
INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF THE FMR1 PROTEIN IN AMALE FRAGILE-X PATIENT WITH A LUNG-TUMOR
Authors: DEGRAAFF E WILLEMSEN R ZHONG N DEDIESMULDERS CEM BROWN WT FRELING G OOSTRA B
Citation: E. Degraaff et al., INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF THE FMR1 PROTEIN IN AMALE FRAGILE-X PATIENT WITH A LUNG-TUMOR, American journal of human genetics, 57(3), 1995, pp. 609-618
FRAGILE-X GENE INSTABILITY - ANCHORING AGGS AND LINKED MICROSATELLITES
Authors: ZHONG N YANG WH DOBKIN C BROWN WT
Citation: N. Zhong et al., FRAGILE-X GENE INSTABILITY - ANCHORING AGGS AND LINKED MICROSATELLITES, American journal of human genetics, 57(2), 1995, pp. 351-361
FRAXAC2 INSTABILITY - REPLY
Authors: ZHONG N DOBKIN C BROWN WT
Citation: N. Zhong et al., FRAXAC2 INSTABILITY - REPLY, Nature genetics, 7(2), 1994, pp. 123-123
POSTNATAL CONFIRMATION OF PRENATALLY DIAGNOSED TRISOMY-16 MOSAICISM IN 2 PHENOTYPICALLY ABNORMAL LIVEBORNS
Authors: PLETCHER BA SANZ MM SCHLESSEL JS KUNAPORN S MCKENNA C BIALER MG ALONSO ML ZASLAV AL BROWN WT RAY JH
Citation: Ba. Pletcher et al., POSTNATAL CONFIRMATION OF PRENATALLY DIAGNOSED TRISOMY-16 MOSAICISM IN 2 PHENOTYPICALLY ABNORMAL LIVEBORNS, Prenatal diagnosis, 14(10), 1994, pp. 933-940
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