[Incidental diagnosis of homozygous alpha-zero thalassemia in a 21 week old fetus].

No abstract is available for this paper.

• Publication year

  1991

• Venue

  Pathologie et biologie

• Publication date

  Unknown publication date

• Fields of study

  Medicine

• Identifiers
  PMID 2011411
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Fetal blood sampling during pregnancy with use of a needle guided by ultrasound: a study of 606 consecutive cases.

  1985cited by this paper
• Isoelectric focusing of human hemoglobin: its application to screening, to the characterization of 70 variants, and to the study of modified fractions of normal hemoglobins.

  1978cited by this paper
• The molecular defects of alpha-thalassemia in the Filipino.

  1977cited by this paper
• Globin synthesis during erythroid cell maturation in alpha thalassemia.

  1976cited by this paper
• The Clinical and Biosynthetic Characterization of αβ‐Thalassaemia

  1972cited by this paper
• Thalassaemia and Hydrops Foetalis—Family Studies

  1967cited by this paper
• A new technique for differentiation of hemoglobin.

  1957cited by this paper

• Hydrops fetalis caused by alpha-thalassemia: an emerging health care problem.

  1998cites this paper
• Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem

  1998cites this paper