Work

Persistent Mullerian duct syndrome caused by both a 27‐bp deletion and a novel splice mutation in the MIS type II receptor gene

Year: 2003

Type: article

Source: Birth Defects Research Part A Clinical and Molecular Teratology

DOI: 10.1002/bdra.10091

Authors: Makiko Hoshiya, Benjamin P. Christian, William J. Cromie, Hyung Kim, Yong Zhan, David T. MacLaughlin, Patricia K. Donahoe

Institutions: Harvard University, Massachusetts General Hospital, University of Chicago Medical Center

Language: English

Topic: Sexual Differentiation and Disorders

Subfield: Molecular Biology

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 Cancer Institute, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G1105990244, G3082707591, Mullerian Inhibiting Substance, MIS RECEPTORS-NOVEL SERINE/THREONINE KINASE COMPONENTS

OpenAlex ID: W2087491822

FWCI: 1.026

Cites: 29

Cited by: 39

Related to: 10