Work

Identification of a submicroscopic deletion of SHH associated with the holoprosencephaly spectrum by array‐based CGH

Year: 2006

Type: article

Source: Clinical Genetics

DOI: 10.1111/j.1399-0004.2006.00598.x

Authors: Jia Huang, Jodi D. Hoffman, Yi Zhang, Melissa K. Maisenbacher, Elaine H. Zackai, Barbara L. Weber, Jeffrey E. Ming

Institutions: University of Pennsylvania, Children's Hospital of Philadelphia

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institute of Dental and Craniofacial Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: Intellectual and Development Disabilities Research Center, G3700531438, Genetic Analysis of Human Holoprosencephaly

OpenAlex ID: W1566530004

FWCI:

Cites: 24

Cited by: 1

Related to: 10