Literature DB >> 6047594

Glucose-6-phosphate dehydrogenase deficiency in female heterozygotes and the X-inactivation hypothesis.

C A Kattamis.   

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Year:  1967        PMID： 6047594     DOI： 10.1111/j.1651-2227.1967.tb15284.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN： 0001-656X


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  4 in total

1.  Favism in breast-fed infants.

Authors:  C Kattamis
Journal:  Arch Dis Child       Date:  1971-10       Impact factor: 3.791

2.  Jaundice and bilirubin levels in Greek children with favism.

Authors:  C Kattamis; K Karambula; V Ioannidou; V Hatzikou
Journal:  Arch Dis Child       Date:  1976-03       Impact factor: 3.791

3.  Heterozygote detection in angiokeratoma corporis diffusum (Anderson-Fabry disease). Studies on plasma, leucocytes, and hair follicles.

Authors:  M W Spence; A L Goldbloom; J K Burgess; D D'entremont; B A Ripley; K L Weldon
Journal:  J Med Genet       Date:  1977-04       Impact factor: 6.318

4.  [Biochemical characterization of a new variant of glucose-6-phosphate dehydrogenase (G-6-PD) deficiency with favism: G-6-PD Bielefeld (author's transl)].

Authors:  M Gahr; D Bornhalm; W Schröter
Journal:  Klin Wochenschr       Date:  1977-04-15
  4 in total

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