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New cases and refinement of the critical region in the 1q41q42 microdeletion syndrome

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Year: 2010
Type: article
Study design: Case Report
Source: European Journal of Medical Genetics
DOI: 10.1016/j.ejmg.2010.10.002
Authors: Jill A. Rosenfeld, Yves Lacassie, Dima El-Khechen, Luis F. Escobar, James Reggin, Carolyn Heuer, Emily Chen, Lauren S. Jenkins, A. Thomas Collins, Samuel Zinner, Melanie Babcock, Bernice Morrow, Roger A. Schultz, Beth S. Torchia, Blake C. Ballif, Karen D. Tsuchiya, Lisa G. Shaffer
Institutions: Louisiana State University, Children's Hospital of New Orleans, Louisiana State University Health Sciences Center New Orleans, St Vincent Hospital, Sacred Heart Medical Center, Kaiser Permanente, Seattle Children's Hospital, University of Washington, Yeshiva University, Albert Einstein College of Medicine
Language: English

Topic: Genomic variations and chromosomal abnormalities
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W2083484048
FWCI: 1.258
Cites: 37
Cited by: 40
Related to: 10
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