Literature DB >> 4164668

Hereditary syndromes with auditory and dermatological manifestations.

W B Reed, V M Stone, E Boder, L Ziprkowski.   

Abstract

Entities:  

Mesh：

Year:  1967        PMID： 4164668

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN： 0003-987X


× No keyword cloud information.
  3 in total

1.  The Bjornstad syndrome (sensorineural hearing loss and pili torti) disease gene maps to chromosome 2q34-36.

Authors:  J F Lubianca Neto; L Lu; R D Eavey; M A Flores; R M Caldera; S Sangwatanaroj; J J Schott; B McDonough; J I Santos; C E Seidman; J G Seidman
Journal:  Am J Hum Genet       Date:  1998-05       Impact factor: 11.025

2.  Hereditary sensorineural hearing loss associated with onychodystrophy and digital malformations.

Authors:  H Moghadam; P Statten
Journal:  Can Med Assoc J       Date:  1972-08-19       Impact factor: 8.262

3.  Bjornstad syndrome.

Authors:  Deepa Aggarwal; Kabir Sardana; Praveen Kumar; Vivek Dewan; V K Anand
Journal:  Indian J Pediatr       Date:  2004-08       Impact factor: 1.967
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.