Publications by authors named "Lisa L Brailey"

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Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Agatino Battaglia, H Eugene Hoyme, Bruno Dallapiccola, Elaine Zackai, Louanne Hudgins, Lisa L Brailey

Pediatrics· February 2008

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Mutations and polymorphisms in the human ornithine transcarbamylase (OTC) gene.
Saori Yamaguchi, Lisa L Brailey, Hiroki Morizono, Allen E Bale, Mendel Tuchman

Hum Mutat· July 2006

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Cardiac and CNS defects in a mouse with targeted disruption of suppressor of fused.
Ayanna F Cooper, Kuan Ping Yu, Martina Brueckner, Lisa L Brailey, Linda Johnson

Development· October 2005

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