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Prenatal diagnosis of Larsen syndrome caused by a mutation in the filamin B gene

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Year: 2008
Type: article
Source: Prenatal Diagnosis
DOI: 10.1002/pd.2164
Authors: N. Winer, F. Kyndt, A. Paumier, A. David, B. Isidor, M. Quentin, B. Jouitteau, P. Sanyas, H. J. Philippe, A. Hernandez, D. Krakow, C. Le Caignec
Institutions: Centre Hospitalier Universitaire de Nantes, Centre National de la Recherche Scientifique, Inserm, Institut du Thorax, Université de Nantes, Nantes Université, Centre Hospitalier de La Rochelle, Cedars-Sinai Medical Center, University of California, Los Angeles
Language: English

Topic: Connective tissue disorders research
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: green

Funders: Centre Hospitalier Universitaire de Nantes, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: G199406178, The Skeletal Dysplasias
OpenAlex ID: W2072441913
FWCI: 1.143
Cites: 10
Cited by: 17
Related to: 10
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