An additional clinical sign of 17q21.31 microdeletion syndrome: Preaxial polydactyly of hands with broad thumbs-Reference-Cited by-同舟云学术

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An additional clinical sign of 17q21.31 microdeletion syndrome: Preaxial polydactyly of hands with broad thumbs

Published:2015-04-09 Issue:7 Volume:167 Page:1671-1673
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Barone Chiara¹,Novelli Antonio²,Capalbo Anna³,del Grano Antonella Cataliotti¹,Giuffrida Maria Grazia³,Indaco Lara¹,Bianca Sebastiano¹

Affiliation:

1. Centro di Consulenza Genetica e Teratologia della Riproduzione; Dipartimento Materno Infantile; ARNAS Garibaldi Nesima Catania Italy

2. Medical Genetics Unit; Bambino Gesù Children's Hospital, IRCCS; Rome Italy

3. Laboratorio Mendel; Roma e Ospedale IRCCS Casa Sollievo della Sofferenza; San Giovanni Rotondo Italy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37054/fullpdf

Reference12 articles.

1. Elements of morphology: standard terminology for the hands and feet;Biesecker;Am J Med Genet PartA,2009

2. Complex phenotype associated with 17q21.31 microdeletion;Dornelles-Wawruk;Mol Syndromol,2013

3. Bifid thumb type IV in children: Transferring an epiphyseal segment of the proximal phalanx with insertion of the abductor pollicis brevis tendon;Hung;J Child Orthop,2010

4. Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome;Koolen;Nat Genet,2012

5. Clinical and molecular delineation of the 17q21.31 microdeletion syndrome;Koolen;J Med Genet,2008

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