Prenatal diagnosis of nonketotic hyperglycinemia
JM García-Castro, CM Isales-Forsythe… - … England Journal of …, 1982 - Mass Medical Soc
Nonketotic hyperglycinemia is a rare autosomal recessive inborn error of glycine
metabolism, characterized by markedly elevated levels of glycine in plasma, urine, and …
metabolism, characterized by markedly elevated levels of glycine in plasma, urine, and …
A new variant of spondylometaphyseal dysplasia with autosomal dominant mode of inheritance.
JM Garcia-Castro, CM Isales-Forsythe… - Journal of Medical …, 1982 - jmg.bmj.com
Clinical and radiographic evaluation of an infant boy and his father revealed findings
suggesting a new variant of spondylometaphyseal dysplasia with an apparently autosomal …
suggesting a new variant of spondylometaphyseal dysplasia with an apparently autosomal …
Prenatal diagnosis of glycine encephalopathy
H Böhles, EC Daly, DB Flannery… - New England …, 1982 - scholars.northwestern.edu
Abstract To the Editor: The report by García-Castro et al.* in the January 14 issue describes
the prenatal diagnosis of nonketotic hyperglycinemia. In 1979 we diagnosed nonketotic …
the prenatal diagnosis of nonketotic hyperglycinemia. In 1979 we diagnosed nonketotic …
[CITATION][C] Lad-V~ lez M, Gonzalez-Rios M, Terres C (1982) Prenal diagnosis of non-ketotic hyperglycinaemia
JM Garcia-Gastro, CM Isales-Forsythe, HL Levy… - N Engl J Med