Literature DB >> 13972696

[Hematological, genetic and clinical observations on some forms of hereditary hemoglobino-pathies (300 cases)].

N QUATTRIN, E DINI.   

Abstract

Entities:  

Keywords:  ANEMIA, ERYTHROBLASTIC; ANEMIA, HYPOCHROMIC; GENETICS, HUMAN; HEMOGLOBINS, ABNORMAL; LIVER CIRRHOSIS; POLYSACCHARIDES

Mesh：

Substances：

Year:  1962        PMID： 13972696

Source DB:  PubMed          Journal:  Schweiz Med Wochenschr        ISSN： 0036-7672


× No keyword cloud information.
  2 in total

1.  New mutation in a Swiss girl leading to clinical and biochemical beta-thalassemia minor.

Authors:  O Tönz; B E Glatthaar; K H Winterhalter; H Ritter
Journal:  Humangenetik       Date:  1973-12-20

2.  [Glucose-6-phosphate dehydrogenase deficiency of erythrocytes in 3 German children. Determination of a new mutation].

Authors:  V Weidtman; O Tönz
Journal:  Klin Wochenschr       Date:  1966-04-15
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.