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
Works matching IS 01973851 AND DT 1989 AND VI 9 AND IP 11
Results: 10
1
2
A 1 and 6 month follow-up of prenatal diagnosis patients who lost pregnancies.
- Published in:
- 1989
- By:
- Publication type:
- journal article
3
Prenatal diagnosis of a case of tetrasomy 9p.
- Published in:
- 1989
- By:
- Publication type:
- journal article
4
Autosomal dominant polycystic kidney disease: prenatal diagnosis by DNA analysis and sonography at 14 weeks.
- Published in:
- 1989
- By:
- Publication type:
- journal article
5
Exophthalmus--prenatal ultrasonic features for diagnosis of Crouzon syndrome.
- Published in:
- 1989
- By:
- Publication type:
- journal article
6
Missed prenatal diagnosis of fragile-X syndrome.
- Published in:
- 1989
- By:
- Publication type:
- journal article
7
Masthead.
- Published in:
- Prenatal Diagnosis, 1989, v. 9, n. 11, p. fmi, doi. 10.1002/pd.1970091101
- Publication type:
- Article
8
Amniotic fluid enzymes in pregnancies with trisomy 21.
- Published in:
- 1989
- By:
- Publication type:
- journal article
9
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
10
In utero ultrasonographic features of campomelic dysplasia.
- Published in:
- 1989
- By:
- Publication type:
- journal article