Literature DB >> 181965

Familial syndrome with dystonia, neural deafness, and possible intellectual impairment: clinical course and pathological findings.

N Scribanu, C Kennedy.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1976        PMID： 181965

Source DB:  PubMed          Journal:  Adv Neurol        ISSN： 0091-3952


× No keyword cloud information.
  3 in total

Review 1.  The genetics of primary torsion dystonia.

Authors:  U Müller; K G Kupke
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

2.  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

3.  Phenotype prediction of Mohr-Tranebjaerg syndrome (MTS) by genetic analysis and initial auditory neuropathy.

Authors:  Hongyang Wang; Li Wang; Ju Yang; Linwei Yin; Lan Lan; Jin Li; Qiujing Zhang; Dayong Wang; Jing Guan; Qiuju Wang
Journal:  BMC Med Genet       Date:  2019-01-11       Impact factor: 2.103
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.