Found: 13
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Masthead.
- Published in:
- Prenatal Diagnosis, 1988, v. 8, n. 3, p. fmi, doi. 10.1002/pd.1970080301
- Publication type:
- Article
Amniotic fluid alpha-fetoprotein levels and prenatal diagnosis of autosomal trisomies.
- Published in:
- 1988
- By:
- Publication type:
- journal article
Microvillar enzyme assays in amniotic fluid and fetal tissues at different stages of development.
- Published in:
- 1988
- By:
- Publication type:
- journal article
Prenatal diagnosis of thalassemia: the viewpoint of patients.
- Published in:
- 1988
- By:
- Publication type:
- journal article
Trisomy 14 mosaicism leading to cytogenetic discrepancies in chorionic villi sampled at different times.
- Published in:
- 1988
- By:
- Publication type:
- journal article
Prenatal diagnosis of 21-hydroxylase deficiency.
- Published in:
- Prenatal Diagnosis, 1988, v. 8, n. 3, p. 245, doi. 10.1002/pd.1970080312
- By:
- Publication type:
- Article
Autosomal recessive polycystic kidney disease. Problems of prenatal diagnosis.
- Published in:
- 1988
- By:
- Publication type:
- journal article
Termination of pregnancy by a dilatation-evacuation technique to obtain placental tissue for DNA analysis.
- Published in:
- 1988
- By:
- Publication type:
- journal article
First trimester diagnosis of methylmalonic aciduria.
- Published in:
- 1988
- By:
- Publication type:
- journal article
Prenatal ultrasound diagnosis of the Holt-Oram syndrome.
- Published in:
- 1988
- By:
- Publication type:
- journal article
Interstitial deletion of chromosome 1 [del(1)(q25q32)] in an infant with prune belly sequence.
- Published in:
- 1988
- By:
- Publication type:
- journal article
Prenatal diagnosis of 21-hydroxylase deficiency.
- Published in:
- Prenatal Diagnosis, 1988, v. 8, n. 3, p. 246, doi. 10.1002/pd.1970080313
- By:
- Publication type:
- Article
First trimester prenatal diagnosis of Sandhoff's disease.
- Published in:
- 1988
- By:
- Publication type:
- journal article