Work

A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients

Year: 2012

Type: article

Study design: Observational Study

Source: International Journal of Pediatric Otorhinolaryngology

DOI: 10.1016/j.ijporl.2012.10.009

Authors: Josine C.C. Widdershoven, Mark Bowser, Molly B. Sheridan, Donna M. McDonald-McGinn, Elaine H. Zackai, Cynthia B. Solot, Richard E. Kirschner, Frits A. Beemer, Bernice E. Morrow, Marcella Devoto, Beverly S. Emanuel

Institutions: Maastricht University Medical Centre, Children's Hospital of Philadelphia, University of Pennsylvania, The Ohio State University, University Medical Center Utrecht, Albert Einstein College of Medicine, Yeshiva University

Language: English

Topic: Cleft Lip and Palate Research

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: National Heart, Lung, and Blood Institute, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: Genetic Modifiers for 22q 11.2 Deletion Syndrome, Developmental mechanisms of human congenital heart disease

OpenAlex ID: W2035559330

FWCI: 0.575

Cites: 31

Cited by: 16

Related to: 10