Triose phosphate isomerase deficiency: Prenatal diagnosis
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference8 articles.
1. Genetic and nongenetic variation of triose phosphate isomerase isozymes in human tissues;Peters;Ann Hum Genet,1973
2. Hereditary hemolytic anemia with triosephosphate isomerase deficiency;Schneider;N Engl J Med,1965
3. Red cell metabolism: A manual of biochemical methods;Beutler,1975
4. Hereditary deficiency of triosephosphate isomerase in four unrelated families;Eber;Eur J Clin Invest,1979
5. Elevated frequency of carriers for triosephosphate isomerase deficiency in newborn infants;Mohreinweiser;Pediatr Res,1982
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1. Other Hereditary Red Blood Cell Disorders;Emery and Rimoin's Principles and Practice of Medical Genetics;2013
2. Triosephosphate isomerase deficiency: biochemical and molecular genetic analysis for prenatal diagnosis;Clinical Genetics;2008-04-23
3. Triosephosphate isomerase deficiency: historical perspectives and molecular aspects;Best Practice & Research Clinical Haematology;2000-03
4. Hereditäre Membrandefekte und Enzymopathien roter Blutzellen;Monogen bedingte Erbkrankheiten 1;2000
5. Triosephosphate Isomerase Deficiency in a Child with Congenital Hemolytic Anemia and Severe Hypotonia;Pediatric Hematology and Oncology;1998-01
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