Work

Identification of new markers in Xp21 between DXS28 (C7) and DMD

Year: 1992

Type: article

Source: Genomics

DOI: 10.1016/0888-7543(92)90007-f

Authors: K.C. Worley, J.A. Towbin, X.M. Zhu, D.F. Barker, A. Ballabio, J. Chamberlain, L.G. Biesecker, S.L. Blethen, P. Brosnan, J.E. Fox, W.B. Rizzo, G. Romeo, N. Sakuragawa, W.K. Seltzer, S. Yamaguchi, E.R.B. McCabe

Institutions: Baylor College of Medicine, University of Utah, University of Michigan, Stony Brook University, Driscoll Children's Hospital, Schneider Children's Hospital, Virginia Commonwealth University Medical Center, Istituto Giannina Gaslini, National Center of Neurology and Psychiatry, University of Colorado Denver, Gifu University

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: green

Funders: National Institutes of Health, National Institute of Child Health and Human Development, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: MOLECULAR GENETIC STUDIES OF GLYCEROL KINASE DEFICIENCY, G1731743910, BAYLOR CHILD HEALTH RESEARCH CENTER, Baylor Intellectual and Developmental Disabilities Research Center, G7872107750, G9000144982, G962945131

OpenAlex ID: W2106897242

FWCI: 2.743

Cites: 20

Cited by: 29

Related to: 10