Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3–q21.2 and screening of the candidate genes-Reference-Cited by-同舟云学术

Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3–q21.2 and screening of the candidate genes

Published:2011-08-30 Issue:3 Volume:131 Page:415-422
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Umm-e-Kalsoom ,Basit Sulman,Kamran-ul-Hassan Naqvi Syed,Ansar Muhammad,Ahmad Wasim

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-011-1085-7.pdf

Reference43 articles.

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3. Buck-Gramcko D (1998) Angeborene Fehlbildungen der Hand. In: Nigst H, Buck-Gramcko D, Milesi H (eds) Handchirurgie. Thieme, Stuttgart, pp 12.1–12.115

4. Cantú JM, del Castillo V, Cortes R, Urrusti J (1974) Autosomal recessive postaxial polydactyly: report of a family. Birth Defects Orig Artic Ser 10:19–22

5. Choi SJ, Moon JH, Ahn YW, Ahn JH, Kim DU, Han TH (2005) Tsc-22 enhances TGF-beta signaling by associating with Smad4 and induces erythroid cell differentiation. Mol Cell Biochem 271:23–28

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