Literature DB >> 5516286

[Heredity of familial oxalosis].

J P Lindenmayer.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1970        PMID： 5516286

Source DB:  PubMed          Journal:  J Genet Hum        ISSN： 0021-7743


× No keyword cloud information.
  2 in total

Review 1.  Primary hyperoxaluria type I.

Authors:  K Latta; J Brodehl
Journal:  Eur J Pediatr       Date:  1990-05       Impact factor: 3.183

2.  Deposition of calcium oxalate in the skin in two patients suffering from oxalosis caused by primary hyperoxaluria.

Authors:  L H Jansen; J L Groeneveld; J B Van Der Meer
Journal:  Arch Dermatol Forsch       Date:  1974
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.