Literature DB >> 13133066

A hereditary factor in chondrodystrophia calcificans congenita.

F C FRASER, J B SCRIVER.   

Abstract

Entities:  

Keywords:  HEREDITY

Mesh:

Year:  1954        PMID: 13133066     DOI: 10.1056/NEJM195402182500702

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


× No keyword cloud information.
  4 in total

1.  Heterogeneity of Chondrodysplasia punctata.

Authors:  J W Spranger; J M Opitz; U Bidder
Journal:  Humangenetik       Date:  1971

2.  Dysplasia spondyloepiphysaria congenita and related generalized skeletal dysplasias among children with severe visual handicaps.

Authors:  G R Fraser; A I Friedmann; P Maroteaux; A M Glen-Bott; U Mittwoch
Journal:  Arch Dis Child       Date:  1969-08       Impact factor: 3.791

Review 3.  Chondrodysplasia punctata: case report and literature review of patients with heart lesions.

Authors:  D T Fourie
Journal:  Pediatr Cardiol       Date:  1995 Sep-Oct       Impact factor: 1.655

4.  Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infants.

Authors:  E F Gilbert; J M Opitz; J W Spranger; L O Langer; J J Wolfson; C Viseskul
Journal:  Eur J Pediatr       Date:  1976-09-01       Impact factor: 3.183

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.