Fetal blood sampling and cytogenetic abnormalities
- 1 January 1993
- journal article
- research article
- Published by Wiley in Prenatal Diagnosis
- Vol. 13 (1) , 1-8
- https://doi.org/10.1002/pd.1970130102
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Postnatal placental confirmation of trisomy 2 and trisomy 16 detected at chorionic villus sampling: A possible association with intrauterine growth retardation and elevated maternal serum alpha‐fetoproteinPrenatal Diagnosis, 1992
- Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndromeCell, 1991
- Mosaic trisomy 16 in a live newborn infant.Archives of Disease in Childhood, 1990
- An embryogenic model to explain cytogenetic inconsistencies observed in chorionic villus versus fetal tissuePrenatal Diagnosis, 1988
- Prenatal Diagnosis of Chromosome AbnormalitiesPublished by Springer Nature ,1986
- Fetal Blood Sampling and FetoscopyPublished by Springer Nature ,1986
- Fetal blood, sampling during pregnancy with use of a needle guided by ultrasound: A study of 606 consecutive casesAmerican Journal of Obstetrics and Gynecology, 1985
- Percutaneous umbilical blood samplingAmerican Journal of Obstetrics and Gynecology, 1985
- Maternal age specific rates for chromosome aberrations and factors influencing them: Report of a collaborative european study on 52 965 amniocentesesPrenatal Diagnosis, 1984
- European collaborative study on prenatal diagnosis: Mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell culturesPrenatal Diagnosis, 1984