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Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndrome

Carrie L Heike1, Jacqueline R Starr, Mark J Rieder

  • 1Department of Pediatrics, Division of Craniofacial Medicine, University of Washington and Seattle Children's Hospital, Seattle, Washington 98105-5371, USA. carrie.heike@seattlechildrens.org

Birth Defects Research. Part A, Clinical and Molecular Teratology
|August 1, 2009
PubMed
Abstract

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