Literature DB >> 13771732

Sex-linked deafness of a possibly new type.

J MOHR, K MAGEROY.   

Abstract

Entities:  

Keywords:  DEAFNESS/genetics

Mesh：

Year:  1960        PMID： 13771732     DOI： 10.1159/000151118

Source DB:  PubMed          Journal:  Acta Genet Stat Med        ISSN： 0567-7440


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  16 in total

1.  X-linked recessive inheritance of sensorineural hearing loss expressed during adolescence.

Authors:  L P Pelletier; R B Tanguay
Journal:  Am J Hum Genet       Date:  1975-09       Impact factor: 11.025

Review 2.  Mitochondrial regulation of cell cycle and proliferation.

Authors:  Valeria Gabriela Antico Arciuch; María Eugenia Elguero; Juan José Poderoso; María Cecilia Carreras
Journal:  Antioxid Redox Signal       Date:  2012-01-13       Impact factor: 8.401

Review 3.  Nonsyndromic hearing impairment: unparalleled heterogeneity.

Authors:  G Van Camp; P J Willems; R J Smith
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

Review 4.  Import of proteins into mitochondria: a novel pathomechanism for progressive neurodegeneration.

Authors:  M F Bauer; W Neupert
Journal:  J Inherit Metab Dis       Date:  2001-04       Impact factor: 4.982

Review 5.  Inherited diseases of the inner ear in man in the light of studies on the mouse.

Authors:  M S Deol
Journal:  J Med Genet       Date:  1968-06       Impact factor: 6.318

6.  Sex-linked congenital deafness.

Authors:  K N McRae; I A Uchida; M Lewis
Journal:  Am J Hum Genet       Date:  1969-09       Impact factor: 11.025

7.  Molecular genetics of a patient with Mohr-Tranebjaerg Syndrome due to a new mutation in the DDP1 gene.

Authors:  José Rafael Blesa; Abelardo Solano; Paz Briones; Jesús Angel Prieto-Ruiz; José Hernández-Yago; Francisco Coria
Journal:  Neuromolecular Med       Date:  2007-08-03       Impact factor: 3.843

8.  Otopathology in Mohr-Tranebjaerg syndrome.

Authors:  Fayez Bahmad; Saumil N Merchant; Joseph B Nadol; Lisbth Tranebjaerg
Journal:  Laryngoscope       Date:  2007-07       Impact factor: 3.325

9.  A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.

Authors:  L Tranebjaerg; C Schwartz; H Eriksen; S Andreasson; V Ponjavic; A Dahl; R E Stevenson; M May; F Arena; D Barker
Journal:  J Med Genet       Date:  1995-04       Impact factor: 6.318

10.  Sex linked deafness: Wilde revisited.

Authors:  W Reardon
Journal:  J Med Genet       Date:  1990-06       Impact factor: 6.318
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