TY  - GEN
AU  - Aitken,D A
AU  - Kleijer,W J
AU  - Niermeijer,M F
AU  - Herbschleb-Voogt,E
AU  - Galjaard,H
TI  - Prenatal detection of a probable heterozygote for ADA deficiency and severe combined immunodeficiency disease using a microradioassay
SN  - 0009-9163
PY  - 1980///0726
KW  - Adenosine Deaminase
KW  - blood
KW  - Amniotic Fluid
KW  - cytology
KW  - Cells, Cultured
KW  - Consanguinity
KW  - Erythrocytes
KW  - enzymology
KW  - Female
KW  - Fetal Blood
KW  - Fibroblasts
KW  - Heterozygote
KW  - Humans
KW  - Immunologic Deficiency Syndromes
KW  - Infant, Newborn
KW  - Microchemistry
KW  - Nucleoside Deaminases
KW  - deficiency
KW  - Phenotype
KW  - Pregnancy
KW  - Prenatal Diagnosis
KW  - Protein Deficiency
KW  - diagnosis
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1111/j.1399-0004.1980.tb00150.x
ER  -