Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)]: Further evidence for phenotypic heterogeneity

Autor:	Philip F. Giampietro, J. Britt Ravnan, Teresa Silberman, David DeBauche, Bhavana J. Dave, Deepti Babu, Carrie Zabel, Ivan Zador
Rok vydání:	2006
Předmět:	Genetics Genetic heterogeneity Biology Genetics (clinical) Genealogy
Zdroj:	American Journal of Medical Genetics Part A. :385-387
ISSN:	1552-4833 1552-4825
DOI:	10.1002/ajmg.a.31067
Popis:	Philip F. Giampietro,* Deepti Babu, Carrie A. Zabel, Teresa Silberman, Ivan Zador, David DeBauche, J. Britt Ravnan, and Bhavana J. Dave Department of Medical Genetic Services, Marshfield, Wisconsin Department of Pediatrics, Marshfield Clinic, Marshfield, Wisconsin Genzyme Genetics, Tampa, Florida Genzyme Genetics, Sante Fe, New Mexico Munroe Meyer Institute for Genetics and Rehabilitation, University of Nebraska Medical Center, Omaha, Nebraska
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::a7a4a3b14f62a3114dcf826dcd8a3bac https://doi.org/10.1002/ajmg.a.31067 Zobrazit plný text záznamu Plný text