A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis-Reference-Cited by-同舟云学术

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

Published:1993-11 Issue:3 Volume:75 Page:443-450
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Jabs Ethylin Wang,Müller Ulrich,Li Xiang,Ma Liang,Luo Wen,Haworth Ian S.,Klisak Ivana,Sparkes Robert,Warman Matthew L.,Mulliken John B.,Snead Malcolm L.,Maxson Rob

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

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