Tandemly repeated DNA sequences of the centromere resulting in 18p +.
- Published in:
- Prenatal Diagnosis, 1989, v. 9, n. 12, p. 863, doi. 10.1002/pd.1970091207
- By:
- Publication type:
- Article
Works matching IS 01973851 AND DT 1989 AND VI 9 AND IP 12
Results: 7
1
2
Familial marker chromosome due to 3:1 Disjunction of t(9;15) in a grandparent.
- Published in:
- Prenatal Diagnosis, 1989, v. 9, n. 12, p. 851, doi. 10.1002/pd.1970091205
- By:
- Publication type:
- Article
3
Amniotic fluid acetylcholinesterase measurement in the prenatal diagnosis of open neural tube defects. Second report of the collaborative acetylcholinesterase study.
- Published in:
- Prenatal Diagnosis, 1989, v. 9, n. 12, p. 813, doi. 10.1002/pd.1970091202
- By:
- Publication type:
- Article
4
A rare case of 68,XX triploidy diagnosed by amniocentesis.
- Published in:
- Prenatal Diagnosis, 1989, v. 9, n. 12, p. 857, doi. 10.1002/pd.1970091206
- By:
- Publication type:
- Article
5
Masthead.
- Published in:
- Prenatal Diagnosis, 1989, v. 9, n. 12, p. fmi, doi. 10.1002/pd.1970091201
- Publication type:
- Article
6
Measurement of HPRT activity in the human unfertilized oocyte and pre-embryo.
- Published in:
- Prenatal Diagnosis, 1989, v. 9, n. 12, p. 839, doi. 10.1002/pd.1970091204
- By:
- Publication type:
- Article
7
Alpha-fetoprotein and acetylcholinesterase in twins discordant for neural tube defect.
- Published in:
- Prenatal Diagnosis, 1989, v. 9, n. 12, p. 831, doi. 10.1002/pd.1970091203
- By:
- Publication type:
- Article