Found: 10
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Prenatal diagnosis of 21-hydroxylase deficiency by RFLP analysis of the 21-hydroxylase, complement C4, and HLA class II genes.
- Published in:
- 1991
- By:
- Publication type:
- journal article
Masthead.
- Published in:
- Prenatal Diagnosis, 1991, v. 11, n. 11, p. fmi, doi. 10.1002/pd.1970111101
- Publication type:
- Article
Clinical and pathological factors in spontaneous abortion following chorionic villus sampling.
- Published in:
- 1991
- By:
- Publication type:
- journal article
A case of mosaicism involving an unstable 13/14 Robertsonian translocation.
- Published in:
- 1991
- By:
- Publication type:
- journal article
Prenatal diagnosis of a fetus with terminal deletion of chromosome 1 (q41)
- Published in:
- 1991
- By:
- Publication type:
- journal article
Trisomy 12 mosaicism.
- Published in:
- 1991
- By:
- Publication type:
- letter
False-negative prenatal exclusion of Wiskott-Aldrich syndrome by measurement of fetal platelet count and size.
- Published in:
- 1991
- By:
- Publication type:
- journal article
Prenatal diagnosis of PIBIDS.
- Published in:
- 1991
- By:
- Publication type:
- journal article
Alpha-fetoprotein and acetylcholinesterase are not predictive of fetal junctional epidermolysis bullosa, Herlitz variant.
- Published in:
- 1991
- By:
- Publication type:
- journal article
Estimating the risk of a fetal autosomal trisomy at mid-trimester using maternal serum alpha-fetoprotein and age: a retrospective study of 142 pregnancies.
- Published in:
- 1991
- By:
- Publication type:
- journal article