Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature
- 1 October 1998
- journal article
- case report
- Published by Wiley in Prenatal Diagnosis
- Vol. 18 (10) , 1055-1060
- https://doi.org/10.1002/(sici)1097-0223(1998100)18:10<1055::aid-pd405>3.0.co;2-i
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- STRUCTURAL CHROMOSOME ANOMALIES IN CONGENITAL DIAPHRAGMATIC HERNIAPrenatal Diagnosis, 1996
- Associated Malformations and Chromosomal Defects in Congenital Diaphragmatic HerniaFetal Diagnosis and Therapy, 1995
- Atrioventricular canal and 8p‐ syndromeAmerican Journal of Medical Genetics, 1993
- Distal 8p deletion (8p23.1----8pter): a common deletion?Journal of Medical Genetics, 1992
- Nonrandom association of atrioventricular canal and del (8p) syndromeAmerican Journal of Medical Genetics, 1992
- Partial monosomy 8p with minimal dysmorphic signs.Journal of Medical Genetics, 1990
- The coagulation factor VII regulator is located on 8p23.1Human Genetics, 1988
- Monosomy 8p: an easily overlooked syndrome.Journal of Medical Genetics, 1986
- Deficiency of chromosome 8p21.1→8pter: Case report and review of the literatureAmerican Journal of Medical Genetics, 1985
- Diaphragmatic hernia in the south-west of England.Journal of Medical Genetics, 1976