A female with complete lack of Müllerian fusion, postaxial polydactyly, and tetralogy of fallot: Genetic heterogeneity of McKusick-Kaufman syndrome or a unique syndrome?-Reference-Cited by-同舟云学术

A female with complete lack of Müllerian fusion, postaxial polydactyly, and tetralogy of fallot: Genetic heterogeneity of McKusick-Kaufman syndrome or a unique syndrome?

Published:2004-03-23 Issue:1 Volume:129A Page:69-72
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Slavotinek Anne M.,Dutra Amalia,Kpodzo Dzifa,Pak Evgenia,Nakane Takaya,Turner Joyce,Whiteford Margo,Biesecker Leslie G.,Stratton Pamela

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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