Work

Microphthalmia with linear skin defects (MLS) syndrome: Clinical, cytogenetic, and molecular characterization

Year: 1994

Type: article

Study design: Case Report

Source: American Journal of Medical Genetics

DOI: 10.1002/ajmg.1320490214

Authors: Elizabeth A. Lindsay, Alessandra Grillo, Giovanni B. Ferrero, Elizabeth J. Roth, Ellen Magenis, Markus Grompe, Maj Hultén, Clive Gould, Antonio Baldini, Huda Y. Zoghbi, Andrea Ballabio

Institutions: Baylor College of Medicine, Oregon Health & Science University

Language: English

Topic: Ocular 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: March of Dimes Foundation, National Institutes of Health, National Human Genome Research Institute, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke

Awards: G1679298920, XIST GENE AND ITS ROLE IN X-INACTIVATION, G5985072634, G6973456568, CLONING OF THE AICARDI AND GOLTZ SYNDROME GENES

OpenAlex ID: W2008201582

FWCI: 3.061

Cites: 25

Cited by: 88

Related to: 10