Work

A man who inherited hisSRY gene and Leri-Weill dyschondrosteosis from his mother and neurofibromatosis type 1 from his father

Year: 2001

Type: article

Study design: Case Report

Source: American Journal of Medical Genetics

DOI: 10.1002/1096-8628(20010901)102:4<353::aid-ajmg1481>3.0.co;2-7

Authors: Fanglin Wei, Sou Cheng, Nicole Badie, Frederick Elder, Charles Scott, Linda Nicholson, Judith L. Ross, Andrew R. Zinn

Institutions: The University of Texas Southwestern Medical Center, Alfred I. duPont Hospital for Children, Thomas Jefferson University

Language: English

Topic: Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: National Institute of Neurological Disorders and Stroke

Award: GENETICS OF COGNITION IN ADULT TURNER SYNDROME

OpenAlex ID: W1969649239

FWCI: 0.345

Cites: 25

Cited by: 22

Related to: 10