Work

PTPN11analysis for the prenatal diagnosis of Noonan syndrome in fetuses with abnormal ultrasound findings

Year: 2009

Type: article

Study design: Observational Study

Source: Clinical Genetics

DOI: 10.1111/j.1399-0004.2008.01085.x

Authors: KA Lee, B Williams, K Roza, H Ferguson, K David, K Eddleman, J Stone, L Edelmann, G Richard, BD Gelb, R Kornreich

Institutions: Icahn School of Medicine at Mount Sinai, Metropolitan Hospital Center

Language: English

Topic: Protein Tyrosine Phosphatases

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 Heart, Lung, and Blood Institute, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G1104865169, SCCOR in Pediatric Heart Development and Disease, G268288826, Disease pathogenesis of Noonan syndrome and related disorders, Molecular Basis of Noonan Syndrome and Related Disorder, G799136563

OpenAlex ID: W2066284262

FWCI: 2.672

Cites: 32

Cited by: 84

Related to: 10