Literature DB >> 5316541

Upington disease: a familial dyschondroplasia.

G Schweitzer, B Jones, A Timme.   

Abstract

Entities:  

Mesh：

Year:  1971        PMID： 5316541

Source DB:  PubMed          Journal:  S Afr Med J


× No keyword cloud information.
  2 in total

1.  Hereditary multiple exostoses.

Authors:  R C Hennekam
Journal:  J Med Genet       Date:  1991-04       Impact factor: 6.318

2.  Epiphyseal dysplasia of the femoral head, mild vertebral abnormality, myopia, and sensorineural deafness: report of a pedigree with autosomal dominant inheritance.

Authors:  K D MacDermot; S C Roth; C Hall; R M Winter
Journal:  J Med Genet       Date:  1987-10       Impact factor: 6.318
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.