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Refinado por: Nome da Publicação: Hum Mol Genet remover assunto: Science & Technology remover Human Molecular Genetics remover
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1
Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions
Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions
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Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions

Yu, Wei ; Ballif, Blake C. ; Kashork, Catherine D. ; Heilstedt, Heidi A. ; Howard, Leslie A. ; Cai, Wei-Wen ; White, Lisa D. ; Liu, Wenbin ; Beaudet, Arthur L. ; Bejjani, Bassem A. ; Shaw, Chad A. ; Shaffer, Lisa G.

Human molecular genetics, 2003-09, Vol.12 (17), p.2145-2152 [Periódico revisado por pares]

Oxford: Oxford University Press

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2
Thiopurine Methyltransferase Alleles in British and Ghanaian Populations
Thiopurine Methyltransferase Alleles in British and Ghanaian Populations
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Thiopurine Methyltransferase Alleles in British and Ghanaian Populations

Ameyaw, Margaret-Mary ; Collie-Duguid, Elaina S. R. ; Powrie, Robert H. ; Ofori-Adjei, David ; McLeod, Howard L.

Human molecular genetics, 1999-02, Vol.8 (2), p.367-370 [Periódico revisado por pares]

Oxford: Oxford University Press

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3
Nuclear Localization of the Spinocerebellar Ataxia Type 7 Protein, Ataxin-7
Nuclear Localization of the Spinocerebellar Ataxia Type 7 Protein, Ataxin-7
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Nuclear Localization of the Spinocerebellar Ataxia Type 7 Protein, Ataxin-7

Kaytor, Michael D. ; Duvick, Lisa A. ; Skinner, Pamela J. ; Koob, Michael D. ; Ranum, Laura P. W. ; Orr, Harry T.

Human molecular genetics, 1999-09, Vol.8 (9), p.1657-1664 [Periódico revisado por pares]

Oxford: Oxford University Press

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4
A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer
A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer
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A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer

Mancini-DiNardo, Debora ; Steele, Scott J.S. ; Ingram, Robert S. ; Tilghman, Shirley M.

Human molecular genetics, 2003-02, Vol.12 (3), p.283-294 [Periódico revisado por pares]

Oxford: Oxford University Press

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5
Chromosome 12q harbors multiple genetic loci related to asthma and asthma-related phenotypes
Chromosome 12q harbors multiple genetic loci related to asthma and asthma-related phenotypes
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Chromosome 12q harbors multiple genetic loci related to asthma and asthma-related phenotypes

Raby, Benjamin A. ; Silverman, Edwin K. ; Lazarus, Ross ; Lange, Christoph ; Kwiatkowski, David J. ; Weiss, Scott T.

Human molecular genetics, 2003-08, Vol.12 (16), p.1973-1979 [Periódico revisado por pares]

Oxford: Oxford University Press

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6
Influence of allele lineage on the role of the insulin minisatellite in susceptibility to type 1 diabetes
Influence of allele lineage on the role of the insulin minisatellite in susceptibility to type 1 diabetes
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Influence of allele lineage on the role of the insulin minisatellite in susceptibility to type 1 diabetes

STEAD, John D. H ; BUARD, Jérome ; TODD, John A ; JEFFREYS, Alec J

Human molecular genetics, 2000-12, Vol.9 (20), p.2929-2935 [Periódico revisado por pares]

Oxford: Oxford University Press

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7
In vivo Nuclease Hypersensitivity Studies Reveal Multiple Sites of Parental Origin-Dependent Differential Chromatin Conformation in the 150 Kb SNRPN Transcription Unit
In vivo Nuclease Hypersensitivity Studies Reveal Multiple Sites of Parental Origin-Dependent Differential Chromatin Conformation in the 150 Kb SNRPN Transcription Unit
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In vivo Nuclease Hypersensitivity Studies Reveal Multiple Sites of Parental Origin-Dependent Differential Chromatin Conformation in the 150 Kb SNRPN Transcription Unit

Schweizer, Johannes ; Zynger, Debra ; Francke, Uta

Human molecular genetics, 1999-04, Vol.8 (4), p.555-566 [Periódico revisado por pares]

Oxford: Oxford University Press

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8
Pharmacogenomics in schizophrenia: the quest for individualized therapy
Pharmacogenomics in schizophrenia: the quest for individualized therapy
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Pharmacogenomics in schizophrenia: the quest for individualized therapy

Basile, Vincenzo S. ; Masellis, Mario ; Potkin, Steven G. ; Kennedy, James L.

Human molecular genetics, 2002-10, Vol.11 (20), p.2517-2530 [Periódico revisado por pares]

Oxford: Oxford University Press

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9
The Pattern of Replication at a Human Telomeric Region (16p13.3): Its Relationship to Chromosome Structure and Gene Expression
The Pattern of Replication at a Human Telomeric Region (16p13.3): Its Relationship to Chromosome Structure and Gene Expression
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The Pattern of Replication at a Human Telomeric Region (16p13.3): Its Relationship to Chromosome Structure and Gene Expression

Smith, Zoe E. ; Higgs, Douglas R.

Human molecular genetics, 1999-08, Vol.8 (8), p.1373-1386 [Periódico revisado por pares]

Oxford: Oxford University Press

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10
Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR
Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR
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Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR

CRAWFORD, Dana C ; WILSON, Beth ; SHERMAN, Stephanie L

Human molecular genetics, 2000-11, Vol.9 (19), p.2909-2918 [Periódico revisado por pares]

Oxford: Oxford University Press

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