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Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure

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Year: 2004
Type: article
Study design: Case Report
Source: European Journal of Human Genetics
DOI: 10.1038/sj.ejhg.5201302
Authors: Marzena Gajecka, Wei Yu, Blake C Ballif, Caron D Glotzbach, Kristen A Bailey, Chad A Shaw, Catherine D Kashork, Heidi A Heilstedt, David A Ansel, Aaron Theisen, Ritva Rice, David P C Rice, Lisa G Shaffer
Institutions: Washington State University Spokane, Baylor College of Medicine, Providence Sacred Heart Medical Center, Boston Children's Hospital, King's College London
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

Funders: National Institute on Deafness and Other Communication Disorders, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: MAPPING AND IDENTIFICATION OF DEAFNESS LOCI TO LP36.3, Chromosome Rearrangements and Mental Retardation
OpenAlex ID: W1984847337
FWCI: 2.479
Cites: 70
Cited by: 148
Related to: 10
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