Work

O.16Diagnosis of fetal akinesia and arthrogryposis by panel sequencing and functional genomics

Year: 2019

Type: article

Study design: Observational Study

Source: Neuromuscular Disorders

DOI: 10.1016/j.nmd.2019.06.296

Authors: G. Ravenscroft, J. Clayton, F. Faiz, D. Milnes, R. Cincotta, P. Moon, P. McGrath, A. Colley, K. Chao, N. Laing, M. Davis

Institutions: The University of Western Australia, Pathwest Laboratory Medicine, Royal Brisbane and Women's Hospital, Mater Mothers' Hospital, Liverpool Hospital, Broad Institute

Language: English

Topic: Genomics and Rare Diseases

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2976211652

FWCI:

Cites:

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