Molecular Syndromology,volume 2,issue 1  (10-2011)

Period of time： 2011年1期

Publisher： Karger

Founded in： 2010

Total resources： 43

E-ISSN： 1661-8777|2|1

ISSN： 1661-8769

Subject： Q3 Genetics

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Molecular Syndromology,volume 2,issue 1

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Osteogenesis Imperfecta: A Review with Clinical Examples

Molecular Syndromology,volume 2,issue 1 , Vol. 2, Iss. 1, 2011-10 , pp. 1-20

Karger

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Dysspondyloenchondromatosis: Another COL2A1-Related Skeletal Dysplasia

Molecular Syndromology,volume 2,issue 1 , Vol. 2, Iss. 1, 2011-10 , pp. 21-26

Karger

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Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies

Molecular Syndromology,volume 2,issue 1 , Vol. 2, Iss. 1, 2011-11 , pp. 27-34

Karger

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22q11.2 Distal Deletion Syndrome: Description of a New Case with Truncus Arteriosus Type 2 and Review

Molecular Syndromology,volume 2,issue 1 , Vol. 2, Iss. 1, 2011-12 , pp. 35-44

Karger

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Severe Developmental Delay in a Patient with 7p21.1–p14.3 Microdeletion Spanning the TWIST Gene and the HOXA Gene Cluster

Molecular Syndromology,volume 2,issue 1 , Vol. 2, Iss. 1, 2011-11 , pp. 45-49

Karger

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Targeting Mitochondria by Olesoxime or Complement 1q Binding Protein as a Novel Management for Autism: A Hypothesis

Molecular Syndromology,volume 2,issue 1 , Vol. 2, Iss. 1, 2011-10 , pp. 50-52

Karger

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Total 6 item(s)