Human Molecular Genetics,volume 7,issue 4  (04-2013)

Period of time： 2013年4期

Publisher： Oxford University Press

Founded in： 1992

Total resources： 344

ISSN： 1460-2083

Subject： Q3 Genetics

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Human Molecular Genetics,volume 7,issue 4

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A sea urchin gene encoding dystrophin-related proteins

By Wang J. in (1998)

Human Molecular Genetics,volume 7,issue 4 , Vol. 7, Iss. 4, 1998-04 , pp. 581-588

Oxford University Press

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Dystrophins in vertebrates and invertebrates

By Roberts R.G.,Bobrow M. in (1998)

Human Molecular Genetics,volume 7,issue 4 , Vol. 7, Iss. 4, 1998-04 , pp. 589-595

Oxford University Press

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IMPT1 , an imprinted gene similar to polyspecific transporter and multi-drug resistance genes

By Dao D. in (1998)

Human Molecular Genetics,volume 7,issue 4 , Vol. 7, Iss. 4, 1998-04 , pp. 597-608

Oxford University Press

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Metaphase fragility of the human RNU1 and RNU2 loci is induced by actinomycin D through a p53-dependent pathway

By Yu A.,Bailey A.D.,Weiner A.M. in (1998)

Human Molecular Genetics,volume 7,issue 4 , Vol. 7, Iss. 4, 1998-04 , pp. 609-617

Oxford University Press

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Identification of four new mutations in the short-chain acyl-CoA dehydrogenase ( SCAD ) gene in two patients: one of the variant alleles, 511C→T, is present at an unexpectedly high frequency in the general population, as was the case for 625G→A, together conferring susceptibility to ethylmalonic aciduria

By Bhala A. in (1998)

Human Molecular Genetics,volume 7,issue 4 , Vol. 7, Iss. 4, 1998-04 , pp. 619-627

Oxford University Press

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ES2 , a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene

By Harvey E.L. in (1998)

Human Molecular Genetics,volume 7,issue 4 , Vol. 7, Iss. 4, 1998-04 , pp. 629-635

Oxford University Press

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The t(8;13)(p11;q11–12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP

By Shipley J. in (1998)

Human Molecular Genetics,volume 7,issue 4 , Vol. 7, Iss. 4, 1998-04 , pp. 637-642

Oxford University Press

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Hypervariable digital DNA codes for human paternal lineages: MVR-PCR at the Y-specific minisatellite, MSY1 ( DYF155S1 )

By Bouzekri N. in (1998)

Human Molecular Genetics,volume 7,issue 4 , Vol. 7, Iss. 4, 1998-04 , pp. 643-653

Oxford University Press

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Novel mutation processes in the evolution of a haploid minisatellite, MSY1: array homogenization without homogenization

By Bouzekri N. in (1998)

Human Molecular Genetics,volume 7,issue 4 , Vol. 7, Iss. 4, 1998-04 , pp. 655-659

Oxford University Press

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Non-disjunction of chromosome 18

By Brøndum-Nielsen K. in (1998)

Human Molecular Genetics,volume 7,issue 4 , Vol. 7, Iss. 4, 1998-04 , pp. 661-669

Oxford University Press

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