Molecular Genetics & Genomic Medicine,volume 3,issue 6  (11-2015)

Period of time： 2015年6期

Publisher： John Wiley & Sons Inc

Founded in： 2012

Total resources： 19

E-ISSN： 2324-9269|3|6

ISSN： 2324-9269

Subject： Q3 Genetics

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Molecular Genetics & Genomic Medicine,volume 3,issue 6

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Molecular Genetics & Genomic Medicine,volume 3,issue 6 , Vol. 3, Iss. 6, 2015-11 , pp. i-iii

John Wiley & Sons Inc

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Foreword to volume 3, issue 6

Molecular Genetics & Genomic Medicine,volume 3,issue 6 , Vol. 3, Iss. 6, 2015-11 , pp. 481-482

John Wiley & Sons Inc

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Remembering Johann Gregor Mendel: a human, a Catholic priest, an Augustinian monk, and abbot

Molecular Genetics & Genomic Medicine,volume 3,issue 6 , Vol. 3, Iss. 6, 2015-11 , pp. 483-485

John Wiley & Sons Inc

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Medical genetics and genomic medicine in Rwanda

Molecular Genetics & Genomic Medicine,volume 3,issue 6 , Vol. 3, Iss. 6, 2015-11 , pp. 486-489

John Wiley & Sons Inc

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Identification of an Alu‐repeat‐mediated deletion of OPTN upstream region in a patient with a complex ocular phenotype

Molecular Genetics & Genomic Medicine,volume 3,issue 6 , Vol. 3, Iss. 6, 2015-11 , pp. 490-499

John Wiley & Sons Inc

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Identification of point mutations and large intragenic deletions in Fanconi anemia using next‐generation sequencing technology

Molecular Genetics & Genomic Medicine,volume 3,issue 6 , Vol. 3, Iss. 6, 2015-11 , pp. 500-512

John Wiley & Sons Inc

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126 novel mutations in Italian patients with neurofibromatosis type 1

Molecular Genetics & Genomic Medicine,volume 3,issue 6 , Vol. 3, Iss. 6, 2015-11 , pp. 513-525

John Wiley & Sons Inc

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Uncovering the molecular pathogenesis of congenital hyperinsulinism by panel gene sequencing in 32 Chinese patients

Molecular Genetics & Genomic Medicine,volume 3,issue 6 , Vol. 3, Iss. 6, 2015-11 , pp. 526-536

John Wiley & Sons Inc

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The rs3737964 single‐nucleotide polymorphism of the chloride channel‐6 gene as a risk factor for coronary heart disease

Molecular Genetics & Genomic Medicine,volume 3,issue 6 , Vol. 3, Iss. 6, 2015-11 , pp. 537-542

John Wiley & Sons Inc

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A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencing

Molecular Genetics & Genomic Medicine,volume 3,issue 6 , Vol. 3, Iss. 6, 2015-11 , pp. 543-549

John Wiley & Sons Inc

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