Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly
- 1 October 1989
- journal article
- review article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 34 (2) , 237-245
- https://doi.org/10.1002/ajmg.1320340222
Abstract
No abstract availableKeywords
This publication has 82 references indexed in Scilit:
- Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic maleHuman Genetics, 1988
- Congenital heart defect in a patient with deletion of chromosome 7qAmerican Journal of Medical Genetics, 1988
- Retinoic Acid EmbryopathyNew England Journal of Medicine, 1985
- Single central incisor in familial holoprosencephalyThe Journal of Pediatrics, 1984
- Holoprosencephaly in infants of diabetic mothersThe Journal of Pediatrics, 1983
- Cyclopia and other anomalies following maternal ingestion of salicylatesThe Journal of Pediatrics, 1980
- The spectrum of the DiGeorge syndromeThe Journal of Pediatrics, 1979
- Familial holoprosencephaly with endocrine dysgenesisThe Journal of Pediatrics, 1968
- Experimental production of perfect cyclopia in the chick by means of LiCl, with a survey of the literature on cyclopia produced experimentally by various meansDevelopmental Biology, 1963
- The Lessons OF RARE MALADIES.: The Annual Oration delivered before the Medical Society of London on May 21st, 1928,The Lancet, 1928