Molecular Syndromology,volume 1,issue 3  (09-2010)

Period of time： 2010年3期

Publisher： Karger

Founded in： 2010

Total resources： 43

E-ISSN： 1661-8777|1|3

ISSN： 1661-8769

Subject： Q3 Genetics

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Molecular Syndromology,volume 1,issue 3

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Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial Diverticulum

Molecular Syndromology,volume 1,issue 3 , Vol. 1, Iss. 3, 2010-09 , pp. 99-112

Karger

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Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A

Molecular Syndromology,volume 1,issue 3 , Vol. 1, Iss. 3, 2010-09 , pp. 113-120

Karger

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Expansion of the Spectrum of FLNA Mutations Associated with Melnick-Needles Syndrome

Molecular Syndromology,volume 1,issue 3 , Vol. 1, Iss. 3, 2010-09 , pp. 121-126

Karger

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A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid Features

Molecular Syndromology,volume 1,issue 3 , Vol. 1, Iss. 3, 2010-09 , pp. 127-132

Karger

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An Illustrative Case of Neurofibromatosis Type 1 and NF1 Microdeletion

Molecular Syndromology,volume 1,issue 3 , Vol. 1, Iss. 3, 2010-09 , pp. 133-135

Karger

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MRNET Conference

Molecular Syndromology,volume 1,issue 3 , Vol. 1, Iss. 3, 2010-09 , pp. 136-157

Karger

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Total 6 item(s)