Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss-Reference-Cited by-同舟云学术

Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss

Published:2015-03-20 Issue:1 Volume:8 Page:
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Iossa Sandra,Costa Valerio,Corvino Virginia,Auletta Gennaro,Barruffo Luigi,Cappellani Stefania,Ceglia Carlo,Cennamo Giovanni,D’Adamo Adamo Pio,D’Amico Alessandra,Di Paolo Nilde,Forte Raimondo,Gasparini Paolo,Laria Carla,Lombardo Barbara,Malesci Rita,Vitale Andrea,Marciano Elio,Franzè Annamaria

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry (medical),Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Link

http://link.springer.com/content/pdf/10.1186/s13039-015-0120-0.pdf

Reference39 articles.

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