The Spectrum of Mutations in TBX3: Genotype/Phenotype Relationship in Ulnar-Mammary Syndrome-Reference-Cited by-同舟云学术

The Spectrum of Mutations in TBX3: Genotype/Phenotype Relationship in Ulnar-Mammary Syndrome

Published:1999-06 Issue:6 Volume:64 Page:1550-1562
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Bamshad M.,Le T.,Watkins W.S.,Dixon M.E.,Kramer B.E.,Roeder A.D.,Carey J.C.,Root S.,Schinzel A.,Van Maldergem L.,Gardner R.J.M.,Lin R.C.,Seidman C.E.,Seidman J.G.,Wallerstein R.,Moran E.,Sutphen R.,Campbell C.E.,Jorde L.B.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference41 articles.

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2. Cloning, mapping, and expression analysis of TBX15, a new member of the T-box gene family;Agulnik;Genomics,1998

3. Basic local alignment search tool;Altschul;J Mol Biol,1990

4. Mutations in human TBX3 alter limb apocrine and genital development in ulnar-mammary syndrome;Bamshad;Nat Genet,1997

5. Clinical analysis of a large kindred with the Pallister ulnar-mammary syndrome;Bamshad;Am J Med Genet,1996

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