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Results: 1-12 |
Results: 12
CONTRIBUTION OF DNA-SEQUENCE AND CAG SIZE TO MUTATION FREQUENCIES OF INTERMEDIATE ALLELES FOR HUNTINGTON DISEASE - EVIDENCE FROM SINGLE SPERM ANALYSES
Authors: CHONG SS ALMQVIST E TELENIUS H LATRAY L NICHOL K BOURDELATPARKS B GOLDBERG YP HADDAD BR RICHARDS F SILLENCE D GREENBERG CR IVES E VANDENENGH G HUGHES MR HAYDEN MR
Citation: Ss. Chong et al., CONTRIBUTION OF DNA-SEQUENCE AND CAG SIZE TO MUTATION FREQUENCIES OF INTERMEDIATE ALLELES FOR HUNTINGTON DISEASE - EVIDENCE FROM SINGLE SPERM ANALYSES, Human molecular genetics, 6(2), 1997, pp. 301-309
DELINEATION OF A DUPLICATION MAP OF CHROMOSOME 3Q - A NEW CASE CONFIRMS THE EXCLUSION OF 3Q25-Q26.2 FROM THE DUPLICATION 3Q SYNDROME CRITICAL REGION
Authors: RIZZU P HADDAD BR VALLCORBA I ALONSO A FERRO MT GARCIASAGREDO JM BALDINI A
Citation: P. Rizzu et al., DELINEATION OF A DUPLICATION MAP OF CHROMOSOME 3Q - A NEW CASE CONFIRMS THE EXCLUSION OF 3Q25-Q26.2 FROM THE DUPLICATION 3Q SYNDROME CRITICAL REGION, American journal of medical genetics, 68(4), 1997, pp. 428-432
APPLICATION OF SPECTRAL KARYOTYPING IN CLINICAL CYTOGENETICS
Authors: HADDAD BR MECK J YOUNG H COWAN J DUMANOIR S SCHROCK E RIED T
Citation: Br. Haddad et al., APPLICATION OF SPECTRAL KARYOTYPING IN CLINICAL CYTOGENETICS, American journal of human genetics, 61(4), 1997, pp. 720-720
DIAGNOSIS OF ANEUPLOIDY IN ARCHIVAL FORMALIN-FIXED PARAFFIN-EMBEDDED PREGNANCY LOSS TISSUES BY COMPARATIVE GENOMIC HYBRIDIZATION
Authors: BELL KA VANDEERLIN PG DUMANOIR S FEINBERG RF HADDAD BR
Citation: Ka. Bell et al., DIAGNOSIS OF ANEUPLOIDY IN ARCHIVAL FORMALIN-FIXED PARAFFIN-EMBEDDED PREGNANCY LOSS TISSUES BY COMPARATIVE GENOMIC HYBRIDIZATION, American journal of human genetics, 61(4), 1997, pp. 834-834
DIFFERENT MUTATION-RATES OF SIMILAR SIZED CAG TRACTS OF AFFECTED HUNTINGTON-DISEASE CHROMOSOMES BY SINGLE SPERM ANALYSIS
Authors: ALMQVIST E CHONG SS NICHOL K TELENIUS H LATRAY L BOURDELATPARKS B HADDAD BR SQUITIERI F ANVRET M VANDENENGH G HAYDEN M
Citation: E. Almqvist et al., DIFFERENT MUTATION-RATES OF SIMILAR SIZED CAG TRACTS OF AFFECTED HUNTINGTON-DISEASE CHROMOSOMES BY SINGLE SPERM ANALYSIS, American journal of human genetics, 61(4), 1997, pp. 1768-1768
EVALUATION OF SATELLITED Y-CHROMOSOME (YQS) DETECTED DURING PRENATAL-DIAGNOSIS
Authors: HADDAD BR HUANG YF WYANDT H MILUNSKY A
Citation: Br. Haddad et al., EVALUATION OF SATELLITED Y-CHROMOSOME (YQS) DETECTED DURING PRENATAL-DIAGNOSIS, Acta obstetricia et gynecologica Scandinavica, 76(3), 1997, pp. 281-283
CUSHINGS-DISEASE PRECEDED BY GENERALIZED GLUCOCORTICOID RESISTANCE - CLINICAL CONSEQUENCES OF A NOVEL, DOMINANT-NEGATIVE GLUCOCORTICOID RECEPTOR MUTATION
Authors: KARL M LAMBERTS SWJ KOPER JW KATZ DA HUIZENGA NE KINO T HADDAD BR HUGHES MR CHROUSOS GP
Citation: M. Karl et al., CUSHINGS-DISEASE PRECEDED BY GENERALIZED GLUCOCORTICOID RESISTANCE - CLINICAL CONSEQUENCES OF A NOVEL, DOMINANT-NEGATIVE GLUCOCORTICOID RECEPTOR MUTATION, Proceedings of the Association of American Physicians, 108(4), 1996, pp. 296-307
MOLECULAR CYTOGENETIC CHARACTERIZATION OF THE FIRST FAMILIAL CASE OF PARTIAL 9P DUPLICATION (P22P24)
Authors: HADDAD BR LIN AE WYANDT H MILUNSKY A
Citation: Br. Haddad et al., MOLECULAR CYTOGENETIC CHARACTERIZATION OF THE FIRST FAMILIAL CASE OF PARTIAL 9P DUPLICATION (P22P24), Journal of Medical Genetics, 33(12), 1996, pp. 1045-1047
MOLECULAR-CLONING OF HUMAN G-ALPHA(Q) CDNA AND CHROMOSOMAL LOCALIZATION OF THE G-ALPHA(Q) GENE (GNAQ) AND A PROCESSED PSEUDOGENE
Authors: DONG QH SHENKER A WAY J HADDAD BR LIN KI HUGHES MR MCBRIDE OW SPIEGEL AM BATTEY J
Citation: Qh. Dong et al., MOLECULAR-CLONING OF HUMAN G-ALPHA(Q) CDNA AND CHROMOSOMAL LOCALIZATION OF THE G-ALPHA(Q) GENE (GNAQ) AND A PROCESSED PSEUDOGENE, Genomics, 30(3), 1995, pp. 470-475
SINGLE-CELL DETECTION OF THE FMR1, HD, AND SCA1 TRINUCLEOTIDE REPEATS- APPLICATION TO PREIMPLANTATION DIAGNOSIS AND INSTABILITY ANALYSIS OF FRAGILE-X SYNDROME, HUNTINGTON DISEASE, AND SPINO-CEREBELLAR ATAXIA TYPE-1
Authors: HUGHES MR HADDAD BR SUBRAMANIAN S NASONKIN I COTA J CHONG SS
Citation: Mr. Hughes et al., SINGLE-CELL DETECTION OF THE FMR1, HD, AND SCA1 TRINUCLEOTIDE REPEATS- APPLICATION TO PREIMPLANTATION DIAGNOSIS AND INSTABILITY ANALYSIS OF FRAGILE-X SYNDROME, HUNTINGTON DISEASE, AND SPINO-CEREBELLAR ATAXIA TYPE-1, American journal of human genetics, 57(4), 1995, pp. 152-152
GENETIC TYPING OF SINGLE CELLS USING MULTIPLE TETRAMERIC TANDEM REPEATS AFTER WHOLE GENOME AMPLIFICATION
Authors: HADDAD BR CHONG SS SUBRAMANIAN S COTA J HUGHES MR
Citation: Br. Haddad et al., GENETIC TYPING OF SINGLE CELLS USING MULTIPLE TETRAMERIC TANDEM REPEATS AFTER WHOLE GENOME AMPLIFICATION, American journal of human genetics, 57(4), 1995, pp. 156-156
SPONTANEOUS CLOSURE OF ENTEROVAGINAL FISTULA CAUSED BY A NEGLECTED FOREIGN-BODY
Authors: HADDAD BR USTA IM KHALIL A MUFARRIJ I
Citation: Br. Haddad et al., SPONTANEOUS CLOSURE OF ENTEROVAGINAL FISTULA CAUSED BY A NEGLECTED FOREIGN-BODY, Acta obstetricia et gynecologica Scandinavica, 73(7), 1994, pp. 598-600
Risultati: 1-12 |