Prenatal diagnosis of 21-hydroxylase deficiency
- 1 March 1988
- journal article
- Published by Wiley in Prenatal Diagnosis
- Vol. 8 (3) , 245-246
- https://doi.org/10.1002/pd.1970080312
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- HLA-D and -DR antigens on human amniotic fluid cells. II. Heterogeneous expression of HLA-DR and other cell surface markersTissue Antigens, 2008
- HLA‐A,B,C,DR typing and 17‐OHP determination for second trimester prenatal diagnosis of 21‐hydroxylase deficient CAHPrenatal Diagnosis, 1988
- HLA typing used with cultured amniotic and chorionic villus cells for early prenatal diagnosis or parentage testing without one parent's availabilityHuman Immunology, 1986
- Lymphocytes recognize human vascular endothelial and dermal fibroblast Ia antigens induced by recombinant immune interferonNature, 1983
- Letter to the editorPrenatal Diagnosis, 1982