Frontonasal “dysplasia,” cerebral anomalies, and polydactyly: Report of a new syndrome and discussion from a developmental field perspective
- 1 January 1986
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 25 (S2) , 89-96
- https://doi.org/10.1002/ajmg.1320250613
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Congenital hypothalamic hamartoma associated with severe midline defect: A developmental field defect. Report of a caseAmerican Journal of Medical Genetics, 1986
- Syndrome of polydactyly, cleft lip, lingual hamartomas, renal hypoplasia, hearing loss, and psychomotor retardation: variant of the Mohr syndrome or a new syndrome?Journal of Medical Genetics, 1983
- Frontonasal dysplasia, coronal cranisoynostosis, pre‐ and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and varibale expression?Clinical Genetics, 1983
- Micromelia, polysyndactyly, multiple malformations, and fragile bones in a stillborn child.Journal of Medical Genetics, 1982
- The acrocallosal syndromeAmerican Journal of Medical Genetics, 1982
- Dandy-Walker Syndrome in Consecutive SiblingsNeurosurgery, 1981
- A familial syndrome of central nervous system and ocular malformationsClinical Genetics, 1975
- Median facial cleft syndrome in half‐sisters. Dilemmas in genetic counselingTeratology, 1973
- Syndrome characterized by lingual malformation, Polydactyly, tachypnea, and psychomotor retardation (Mohr syndrome)Clinical Genetics, 1971
- Frontonasal dysplasiaThe Journal of Pediatrics, 1970