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An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3–Xp21.3

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Year: 1995
Type: article
Source: Human Molecular Genetics
DOI: 10.1093/hmg/4.10.1821
Authors: Glovanni B. Ferrero, Brunella Franco, E.Jill Roth, Beth A. Firulli, Gluseppe Borsanl, Juan Delmas-Mata, Jean Weissenbach, George Halley, David Schlessinger, A.Craig Chinault, Huda Y.Zoghbi, David L.Nelson, Andrea Ballabio
Institutions: Baylor College of Medicine, Genethon (France), Washington University in St. Louis, University of Siena
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 Institutes of Health, National Human Genome Research Institute, National Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: G1679298920, G2531601546, CLONING OF DISEASE GENES FROM THE HUMAN XP22.3 REGION, G4128283354, CLONING OF THE AICARDI AND GOLTZ SYNDROME GENES
OpenAlex ID: W2113604755
FWCI: 7.699
Cites:
Cited by: 74
Related to: 10
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