Trisomy 15 in chorionic villi and Prader-Willi syndrome at birth
- 1 April 1993
- journal article
- Published by Wiley in Prenatal Diagnosis
- Vol. 13 (4) , 307-308
- https://doi.org/10.1002/pd.1970130410
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Genomic Imprinting and Its Clinical ImplicationsNew England Journal of Medicine, 1992
- Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15New England Journal of Medicine, 1992
- Genomic imprinting in an Angelman and Prader-Willi translocation familyThe Lancet, 1991
- Cytogenetic results of chorionic villus sampling: High success rate and diagnostic accuracy in the United States collaborative studyAmerican Journal of Obstetrics and Gynecology, 1990
- Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader‐Willi syndromeAmerican Journal of Medical Genetics, 1989
- An embryogenic model to explain cytogenetic inconsistencies observed in chorionic villus versus fetal tissuePrenatal Diagnosis, 1988
- Confined chorionic mosaicism in prenatal diagnosisHuman Genetics, 1987
- Chromosomal Mosaicism Confined to the Placenta in Human ConceptionsScience, 1983