Chromosome imbalances in syndromic hearing loss-Reference-Cited by-同舟云学术

Chromosome imbalances in syndromic hearing loss

Published:2009-11 Issue:5 Volume:76 Page:458-464
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Catelani ALPM,Krepischi ACV,Kim CA,Kok F,Otto PA,Auricchio MTBM,Mazzeu JF,Uehara DT,Costa SS,Knijnenburg J,Tabith A,Vianna-Morgante AM,Mingroni-Netto RC,Rosenberg C

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2009.01276.x/fullpdf

Reference27 articles.

1. Genes responsible for human hereditary deafness: symphony of a thousand;Petit;Nat Genet,1996

2. Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents;Rosenberg;J Med Genet,2006

3. Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities;Vissers;Am J Hum Genet,2003

4. Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability.;Shaw-Smith;Nat Genet,2006

5. The PDS gene, Pendred syndrome and non-syndromic deafness DFNB4;Wilcox;Adv Otorhinolaryngol,2000

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3. Genomic copy number alterations in non-syndromic hearing loss;Clinical Genetics;2015-11-10

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