Syndromic craniosynostosis associated with microdeletion of chromosome 19p13.12-19p13.2.

Lyon, Sarah M; Waggoner, Darrel; Halbach, Sara; Thorland, Erik C; Khorasani, Leila; Reid, Russell R

Lyon, Sarah M; Waggoner, Darrel; Halbach, Sara; Thorland, Erik C; Khorasani, Leila; Reid, Russell R.

Afiliación

Lyon SM; Pritzker School of Medicine, University of Chicago.
Waggoner D; Department of Human Genetics and Pediatrics, University of Chicago, 5841 S. Maryland Ave, M/C 0077, Chicago, IL 60637.
Halbach S; Department of Human Genetics and Pediatrics, University of Chicago, 5841 S. Maryland Ave, M/C 0077, Chicago, IL 60637.
Thorland EC; Lab Medicine & Pathology, 200 First St SW, Hilton 970, Rochester, MN 55905-0001.
Khorasani L; Department of Surgery, University of Chicago, 5841 S. Maryland Ave, M/C 0077, Chicago, IL 60637.
Reid RR; Department of Surgery, University of Chicago, 5841 S. Maryland Ave, M/C 0077, Chicago, IL 60637.

Genes Dis ; 2(4): 347-352, 2015 Dec.

Article en En | MEDLINE | ID: mdl-26966713

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Genes Dis Año: 2015 Tipo del documento: Article

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