Literature DB >> 13872585

Familial nephrosis associated with deafness and congenital urinary tract anomalies in siblings.

F C BRAUN, J F BAYER.   

Abstract

Entities:  

Keywords:  DEAFNESS/genetics; NEPHROSIS/genetics; UROGENITAL SYSTEM/abnormalities

Mesh：

Year:  1962        PMID： 13872585     DOI： 10.1016/s0022-3476(62)80005-5

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


× No keyword cloud information.
  2 in total

1.  A new syndrome of autosomal recessive nephropathy, deafness, and hyperparathyroidism.

Authors:  B D Edwards; M A Patton; S A Dilly; J B Eastwood
Journal:  J Med Genet       Date:  1989-05       Impact factor: 6.318

2.  Conductive hearing loss and malformed low-set ears, as a possible recessive syndrome.

Authors:  M C Mengel; B W Konigsmark; C I Berlin; V A McKusick
Journal:  J Med Genet       Date:  1969-03       Impact factor: 6.318
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.