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Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome

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Year: 2000
Type: article
Source: Mammalian Genome
DOI: 10.1007/s003350010193
Authors: Russell A. Norris, Karen K. Scott, Clara S. Moore, Gail Stetten, Cuyler R. Brown, Ethylin Wang Jabs, Eric A. Wulfsberg, Jack Yu, Michael J. Kern
Institutions: Medical University of South Carolina, Johns Hopkins University, Johns Hopkins Medicine, University of Maryland, Baltimore, Augusta University
Language: English

Topic: Craniofacial Disorders and Treatments
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of Dental and Craniofacial Research
Awards: G1380091538, HOMEBOX GENES IN CARDIAC DEVELOPMENT AND FUNCTION, G2814367823, G3631997825, MOLECULAR STUDIES OF MANDIBULOFACIAL DYSOSTOSIS, CENTER FOR CRANIOFACIAL DEVELOPMENT AND DISORDERS
OpenAlex ID: W2071985567
FWCI: 0.777
Cites: 39
Cited by: 49
Related to: 10
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