Literature DB >> 13821047

Further studies on hereditary unilateral deafness.

G EVERBERG.   

Abstract

Entities:  

Keywords:  DEAFNESS/genetics

Mesh：

Year:  1960        PMID： 13821047     DOI： 10.3109/00016486009124539

Source DB:  PubMed          Journal:  Acta Otolaryngol        ISSN： 0001-6489            Impact factor:   1.494


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  2 in total

1.  [On unilateral deafness in childhood].

Authors:  E LEHNHARDT
Journal:  Arch Ohren Nasen Kehlkopfheilkd       Date:  1962

2.  Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2.

Authors:  Celia Zazo Seco; Luciana Serrão de Castro; Josephine W van Nierop; Matías Morín; Shalini Jhangiani; Eva J J Verver; Margit Schraders; Nadine Maiwald; Mieke Wesdorp; Hanka Venselaar; Liesbeth Spruijt; Jaap Oostrik; Jeroen Schoots; Jeroen van Reeuwijk; Stefan H Lelieveld; Patrick L M Huygen; María Insenser; Ronald J C Admiraal; Ronald J E Pennings; Lies H Hoefsloot; Alejandro Arias-Vásquez; Joep de Ligt; Helger G Yntema; Joop H Jansen; Donna M Muzny; Gerwin Huls; Michelle M van Rossum; James R Lupski; Miguel Angel Moreno-Pelayo; Henricus P M Kunst; Hannie Kremer
Journal:  Am J Hum Genet       Date:  2015-10-29       Impact factor: 11.025
  2 in total

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