Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1969 Sep;6(3):281–285. doi: 10.1136/jmg.6.3.281

G6PD deficiency in two autochthonous Croatian families.

D Juricić, V Vince-Ribarić, I Ruzdić, S Vuletić
PMCID: PMC1468733  PMID: 5345100

Full text

PDF
282

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Fraser G. R., Grunwald P., Stamatoyannopoulos G. Glucose-6-phosphate dehydrogenase (G6PD) deficiency, abnormal haemoglobins, and thalassaemia in Yugoslavia. J Med Genet. 1966 Mar;3(1):35–41. doi: 10.1136/jmg.3.1.35. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. LYON M. F. Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature. 1961 Apr 22;190:372–373. doi: 10.1038/190372a0. [DOI] [PubMed] [Google Scholar]
  3. SZEINBERG A., ASHER Y., SHEBA C. Studies on glutathione stability in erythrocytes of cases with past history of favism or sulfa-drug-induced hemolysis. Blood. 1958 Apr;13(4):348–358. [PubMed] [Google Scholar]
  4. VINCE-RIBARIC V. [Clinical contribution to the study of favism]. Lijec Vjesn. 1962 Feb;84:151–157. [PubMed] [Google Scholar]
  5. ZINKHAM W. H. An in-vitro abnormality of glutathione metabolism in erythrocytes from normal newborns: mechanism and clinical significance. Pediatrics. 1959 Jan;23(1 Pt 1):18–32. [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES