Literature DB >> 13425596

[Studies on the inner ear of a deaf domestic mouse mutant with motor disorders in comparison with hereditary labyrinthine hearing disorders in man].

H FISCHER.   

Abstract

Entities:  

Keywords:  HEARING DISORDERS/etiology and pathogenesis; LABYRINTH/abnormalities

Mesh：

Year:  1957        PMID： 13425596

Source DB:  PubMed          Journal:  Arch Ohren Nasen Kehlkopfheilkd        ISSN： 0365-5245


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  2 in total

1.  Bone growth: a study of the grey-lethal and microphthalmic mutants of the mouse.

Authors:  N BATEMAN
Journal:  J Anat       Date:  1954-04       Impact factor: 2.610

2.  [Dreher, a new gene of the waltzer-shaker group in the house mouse].

Authors:  D S FALCONER; U SIERTS-ROTH
Journal:  Z Indukt Abstamm Vererbungsl       Date:  1951
  2 in total
  4 in total

1.  [Cochlear defects].

Authors:  H J Paulsen; K W Frey
Journal:  Arch Klin Exp Ohren Nasen Kehlkopfheilkd       Date:  1968

2.  [Studies on the genetics and pathology of the development of 8 labyrinth mutants (deaf-waltzer-shaker mutants) in the mouse (Mus musculus)].

Authors:  W KOCHER
Journal:  Z Vererbungsl       Date:  1960

3.  [Research on the genetics and pathology of the development of delayed hereditary deafness in the mouse (Mus musculus)].

Authors:  W KOCHER
Journal:  Arch Ohren Nasen Kehlkopfheilkd       Date:  1960

4.  Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) are two new mutations of Lmx1a causing severe cochlear and vestibular defects.

Authors:  Georg Steffes; Beatriz Lorente-Cánovas; Selina Pearson; Rachael H Brooker; Sarah Spiden; Amy E Kiernan; Jean-Louis Guénet; Karen P Steel
Journal:  PLoS One       Date:  2012-11-30       Impact factor: 3.240
  4 in total

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