Found: 10
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In utero ultrasonographic features of campomelic dysplasia.
- Published in:
- 1989
- By:
- Publication type:
- journal article
Autosomal dominant polycystic kidney disease: prenatal diagnosis by DNA analysis and sonography at 14 weeks.
- Published in:
- 1989
- By:
- Publication type:
- journal article
Prenatal diagnosis of adult polycystic kidney disease with DNA markers on chromosome 16 and the genetic heterogeneity problem.
- Published in:
- 1989
- By:
- Publication type:
- journal article
Amniotic fluid enzymes in pregnancies with trisomy 21.
- Published in:
- 1989
- By:
- Publication type:
- journal article
Missed prenatal diagnosis of fragile-X syndrome.
- Published in:
- 1989
- By:
- Publication type:
- journal article
Prenatal diagnosis of Opitz (BBB) syndrome in the second trimester by ultrasound detection of hypospadias and hypertelorism.
- Published in:
- 1989
- By:
- Publication type:
- journal article
A 1 and 6 month follow-up of prenatal diagnosis patients who lost pregnancies.
- Published in:
- 1989
- By:
- Publication type:
- journal article
Exophthalmus--prenatal ultrasonic features for diagnosis of Crouzon syndrome.
- Published in:
- 1989
- By:
- Publication type:
- journal article
Prenatal diagnosis of a case of tetrasomy 9p.
- Published in:
- 1989
- By:
- Publication type:
- journal article
Masthead.
- Published in:
- Prenatal Diagnosis, 1989, v. 9, n. 11, p. fmi, doi. 10.1002/pd.1970091101
- Publication type:
- Article