Multigenerational autosomal dominant inheritance of 5p chromosomal deletions

Author:

Zhang Bin1,Willing Marcia2,Grange Dorothy K.2,Shinawi Marwan2,Manwaring Linda2,Vineyard Marisa2,Kulkarni Shashikant1,Cottrell Catherine E.1

Affiliation:

1. Department of Pathology and Immunology; Washington University School of Medicine; Saint Louis Missouri

2. Division of Genetics and Genomic Medicine, Department of Pediatrics; Washington University School of Medicine; Saint Louis Missouri

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference29 articles.

1. The clinical significance of small copy number variants in neurodevelopmental disorders;Asadollahi;J Med Genet,2014

2. Cri du Chat syndrome;Cerruti;Orphanet J Rare Dis,2006

3. An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk;Cheng;Hum Mol Genet,2013

4. Molecular definition of deletions of different segments of distal 5p that result in distinct phenotypic features;Church;Am J Hum Genet,1995

5. A high-resolution physical and transcript map of the Cri du chat region of human chromosome 5p;Church;Genome Res,1997

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