Molecular Genetics & Genomic Medicine,volume 3,issue 3  (05-2015)

Period of time： 2015年3期

Publisher： John Wiley & Sons Inc

Founded in： 2012

Total resources： 19

E-ISSN： 2324-9269|3|3

ISSN： 2324-9269

Subject： Q3 Genetics

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Molecular Genetics & Genomic Medicine,volume 3,issue 3

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Molecular Genetics & Genomic Medicine,volume 3,issue 3 , Vol. 3, Iss. 3, 2015-05 , pp. i-iii

John Wiley & Sons Inc

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Perspectives on what is needed to implement genomic medicine

Molecular Genetics & Genomic Medicine,volume 3,issue 3 , Vol. 3, Iss. 3, 2015-05 , pp. 155-159

John Wiley & Sons Inc

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Medical genetics and genomic medicine in India: current status and opportunities ahead

Molecular Genetics & Genomic Medicine,volume 3,issue 3 , Vol. 3, Iss. 3, 2015-05 , pp. 160-171

John Wiley & Sons Inc

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Distribution of fragile X mental retardation 1 CGG repeat and flanking haplotypes in a large Chinese population

Molecular Genetics & Genomic Medicine,volume 3,issue 3 , Vol. 3, Iss. 3, 2015-05 , pp. 172-181

John Wiley & Sons Inc

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Quantifying the cumulative effect of low‐penetrance genetic variants on breast cancer risk

Molecular Genetics & Genomic Medicine,volume 3,issue 3 , Vol. 3, Iss. 3, 2015-05 , pp. 182-188

John Wiley & Sons Inc

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Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing

Molecular Genetics & Genomic Medicine,volume 3,issue 3 , Vol. 3, Iss. 3, 2015-05 , pp. 189-196

John Wiley & Sons Inc

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Identification of novel mutations in Mexican patients with Aarskog–Scott syndrome

Molecular Genetics & Genomic Medicine,volume 3,issue 3 , Vol. 3, Iss. 3, 2015-05 , pp. 197-202

John Wiley & Sons Inc

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Unraveling the pathogenesis of ARX polyalanine tract variants using a clinical and molecular interfacing approach

Molecular Genetics & Genomic Medicine,volume 3,issue 3 , Vol. 3, Iss. 3, 2015-05 , pp. 203-214

John Wiley & Sons Inc

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Contiguous mutation syndrome in the era of high‐throughput sequencing

Molecular Genetics & Genomic Medicine,volume 3,issue 3 , Vol. 3, Iss. 3, 2015-05 , pp. 215-220

John Wiley & Sons Inc

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Functional consequences of transferrin receptor‐2 mutations causing hereditary hemochromatosis type 3

Molecular Genetics & Genomic Medicine,volume 3,issue 3 , Vol. 3, Iss. 3, 2015-05 , pp. 221-232

John Wiley & Sons Inc

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