Delayed Mutation as a Cause of Genetic Disease in Man: Achondroplasia and the Wiedemann-Beckwith Syndrome
- 1 January 1977
- book chapter
- Published by Springer Nature
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Studies of malformation syndromes of man XXIX: The Wiedemann-Beckwith syndromeEuropean Journal of Pediatrics, 1976
- AUTOSOMAL-DOMINANT SEX-DEPENDENT TRANSMISSION OF THE WIEDEMANN-BECKWITH SYNDROMEThe Lancet, 1974
- WIEDEMANN-BECKWITH SYNDROMEThe Lancet, 1973
- Exomphalos-Makroglossie-Gigantismus-Syndrom, Berardinelli-Seip-Syndrom und Sotos-Syndrom —eine vergleichende Betrachtung unter ausgewählten AspektenEuropean Journal of Pediatrics, 1973
- The Beckwith-Wiedemann SyndromeAmerican Journal of Diseases of Children, 1971
- Achondroplasia—a genetic and statistical surveyAnnals of Human Genetics, 1970
- Exomphalos with macroglossia: A study of eleven casesJournal of Pediatric Surgery, 1967
- A POSSIBLE CASE OF DELAYED MUTATION IN MANAnnals of Human Genetics, 1956