Prenatally diagnosed neural tube defects: Ultrasound, chromosome, and autopsy or postnatal findings in 212 cases
- 26 May 1998
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 77 (4) , 317-321
- https://doi.org/10.1002/(sici)1096-8628(19980526)77:4<317::aid-ajmg13>3.0.co;2-l
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Neural tube defects and deletions of 22q11American Journal of Medical Genetics, 1996
- Aneuploidy among prenatally detected neural tube defectsAmerican Journal of Medical Genetics, 1996
- Prenatal Ultrasound Detection of Isolated Neural Tube Defects: Is Cytogenetic Evaluation Warranted?Published by Wolters Kluwer Health ,1995
- Prenatally detected fetal myelomeningocele: is karyotype analysis warranted?Radiology, 1995
- Evidence for multi‐site closure of the neural tube in humansAmerican Journal of Medical Genetics, 1993
- Significance of a single umbilical artery in fetuses with central nervous system malformations.Journal of Ultrasound in Medicine, 1988
- Monozygosity and holoprosencephaly: Cleavage disorders of the “midline field”American Journal of Medical Genetics, 1987
- Monozygotic twinning and structural defectsThe Journal of Pediatrics, 1979