Variability in the clinical manifestations of galactosemia

Author:

Hsia David Yi-Yung,Walker Frank A.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference20 articles.

1. Some Disturbances of Erythrocyte Metabolism in Galactosemia;Schwarz;Biochem. J.,1956

2. Galactosemia, a Congenital Defect in Nucleotide Transferase;Kalckar;Biochim. et biophys. acta,1956

3. Walker, F. A., Hsia, D. Y. Y., Slatis, H., and Steinberg, A. G.: Galactosemia: A Study of 27 Kindreds in North America, Ann. Human Genet. (in press).

4. A Procedure for Detecting Carriers of Galactosemia;Bretthauer;Proc. Nat. Acad. Sc.,1959

5. Enzymic Evidence of a Galactosemic Trait in Parents of Galactosemic Children;Kirkman;Ann. Human Genet.,1959

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