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Identification of novel mutations in SHH and ZIC2 in a South American (ECLAMC) population with holoprosencephaly

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Year: 2001
Type: article
Study design: Observational Study
Source: Human Genetics
DOI: 10.1007/s004390100537
Authors: Iêda M. Orioli, Eduardo E. Castilla, Jeffrey E. Ming, Julio Nazer, Marcos J. Burle de Aguiar, Juan C. Llerena, Maximilian Muenke
Institutions: Children's Hospital of Philadelphia, University of Pennsylvania, Instituto Oswaldo Cruz, Hospital Clínico de la Universidad de Chile, University of Chile, Hospital das Clínicas da Universidade Federal de Minas Gerais, Instituto Nacional de Saúde da Mulher, da Criança e do Adolescente Fernandes Figueira, Fundação Oswaldo Cruz
Language: English

Topic: Fetal and Pediatric Neurological Disorders
Subfield: Pediatrics, Perinatology and Child Health
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: Conselho Nacional de Desenvolvimento Científico e Tecnológico, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: PATTERNING THE DEVELOPING BRAIN, GENETIC ANALYSIS OF HUMAN BRAIN DEVELOPMENT
OpenAlex ID: W2019829030
FWCI: 4.604
Cites: 14
Cited by: 45
Related to: 10
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