Molecular Genetics & Genomic Medicine,volume 4,issue 1  (01-2016)

Period of time： 2016年1期

Publisher： John Wiley & Sons Inc

Founded in： 2012

Total resources： 19

E-ISSN： 2324-9269|4|1

ISSN： 2324-9269

Subject： Q3 Genetics

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Molecular Genetics & Genomic Medicine,volume 4,issue 1

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Molecular Genetics & Genomic Medicine,volume 4,issue 1 , Vol. 4, Iss. 1, 2016-01 , pp. 1-2

John Wiley & Sons Inc

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Johann Gregor Mendel: paragon of experimental science

Molecular Genetics & Genomic Medicine,volume 4,issue 1 , Vol. 4, Iss. 1, 2016-01 , pp. 3-8

John Wiley & Sons Inc

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Genetics and genomic medicine in Ecuador

Molecular Genetics & Genomic Medicine,volume 4,issue 1 , Vol. 4, Iss. 1, 2016-01 , pp. 9-17

John Wiley & Sons Inc

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Evaluation of genetic association of neurodevelopment and neuroimmunological genes with antipsychotic treatment response in schizophrenia in Indian populations

Molecular Genetics & Genomic Medicine,volume 4,issue 1 , Vol. 4, Iss. 1, 2016-01 , pp. 18-27

John Wiley & Sons Inc

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The dentin phosphoprotein repeat region and inherited defects of dentin

Molecular Genetics & Genomic Medicine,volume 4,issue 1 , Vol. 4, Iss. 1, 2016-01 , pp. 28-38

John Wiley & Sons Inc

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CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome

Molecular Genetics & Genomic Medicine,volume 4,issue 1 , Vol. 4, Iss. 1, 2016-01 , pp. 39-45

John Wiley & Sons Inc

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Fam83h null mice support a neomorphic mechanism for human ADHCAI

Molecular Genetics & Genomic Medicine,volume 4,issue 1 , Vol. 4, Iss. 1, 2016-01 , pp. 46-67

John Wiley & Sons Inc

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Allelic variants of the Melanocortin 4 receptor (MC4R) gene in a South African study group

Molecular Genetics & Genomic Medicine,volume 4,issue 1 , Vol. 4, Iss. 1, 2016-01 , pp. 68-76

John Wiley & Sons Inc

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Hutterite‐type cataract maps to chromosome 6p21.32‐p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac death

Molecular Genetics & Genomic Medicine,volume 4,issue 1 , Vol. 4, Iss. 1, 2016-01 , pp. 77-94

John Wiley & Sons Inc

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Mid1/Mid2 expression in craniofacial development and a literature review of X‐linked opitz syndrome

Molecular Genetics & Genomic Medicine,volume 4,issue 1 , Vol. 4, Iss. 1, 2016-01 , pp. 95-105

John Wiley & Sons Inc

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