A case report of chromosome 17q22-qter trisomy with distinct clinical presentation and review of the literature-Reference-Cited by-同舟云学术

A case report of chromosome 17q22-qter trisomy with distinct clinical presentation and review of the literature

Published:2018-02-14 Issue:4 Volume:6 Page:612-616
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Upadia Jariya¹^ORCID,Philips Joseph B.²,Robin Nathaniel H.¹,Lose Edward J.¹,Mikhail Fady M.¹

Affiliation:

1. Department of Genetics; University of Alabama at Birmingham; Birmingham Alabama USA

2. Department of Pediatrics; University of Alabama at Birmingham; Birmingham Alabama USA

Publisher

Wiley

Subject

General Medicine

Reference24 articles.

1. Duplication (partial trisomy) of the distal long arm of chromosome 17: a new clinically recognizable chromosome disorder;Berberich;Birth Defects Orig Artic. Ser.,1978

2. Brief Clinical report: an infant with duplication of 17q21-17qter;Gallien;Am. J. Med. Genet.,1981

3. Sibs lacking characteristic features of duplication of distal 17q;Ohdo;J. Med. Genet.,1989

4. Distal trisomy 17q;Turleau;Clin. Genet.,1979

5. Clinical characteristics associated with dup17(q24-q25.1) in a mosaic mother and two non-mosaic daughters;Babovic-Vuksanovic;Clin. Dysmorphol.,1998

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