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Antenatal diagnosis of rhizomelic chondrodysplasia punctata in the second trimester
Author(s) -
Gray R. G. F.,
Green A.,
Schutgens R. B. H.,
Wanders R. J. A.,
Farndon P. A.,
Kennedy C. R.
Publication year - 1990
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/bf01799400
Subject(s) - chondrodysplasia punctata , prenatal diagnosis , medicine , human genetics , peroxisomal disorder , pregnancy , metabolic disease , obstetrics , pediatrics , endocrinology , genetics , fetus , biology , anatomy , peroxisome , receptor , gene