Literature DB >> 13897100

Glucose-6-phosphate dehydrogenase deficiency in an XO individual.

S M GARTLER, C VULLO, E GANDINI.   

Abstract

Entities:  

Keywords:  CHROMOSOMES; DEHYDROGENASES/blood; TURNER'S SYNDROME/genetics

Mesh:

Substances:

Year:  1962        PMID: 13897100     DOI: 10.1159/000129708

Source DB:  PubMed          Journal:  Cytogenetics        ISSN: 0011-4537


× No keyword cloud information.
  2 in total

1.  TURNER'S SYNDROME, TWINNING, AND AN UNUSUAL VARIANT OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE.

Authors:  W E NANCE; I UCHIDA
Journal:  Am J Hum Genet       Date:  1964-09       Impact factor: 11.025

2.  Quantitation of phospholipid analysis using P32 by a digital computer method in metabolic experiments on Niemann-Pick disease.

Authors:  A I Holtz
Journal:  J Am Oil Chem Soc       Date:  1967-02       Impact factor: 1.849

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.