Paternal Origin of FGFR2 Mutations in Sporadic Cases of Crouzon Syndrome and Pfeiffer Syndrome
Open Access
- 1 March 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 66 (3), 768-777
- https://doi.org/10.1086/302831
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Clinical spectrum of fibroblast growth factor receptor mutationsHuman Mutation, 1999
- Clinical Features of Crouzonʼs Syndrome Patients With and Without a Positive Family History of Crouzonʼs SyndromeThe Journal of Craniofacial Surgery, 1997
- Exclusive paternal origin of new mutations in Apert syndromeNature Genetics, 1996
- Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosisAmerican Journal of Medical Genetics, 1993
- Birth prevalence studies of the Crouzon syndrome: comparison of direct and indirect methodsClinical Genetics, 1992
- On the parental origin of de novo mutation in man.Journal of Medical Genetics, 1991
- Fluorescence detection in automated DNA sequence analysisNature, 1986
- Older paternal age and fresh gene mutation: Data on additional disordersThe Journal of Pediatrics, 1975
- Spermatogenesis in Man: An Estimate of Its DurationScience, 1963
- PARENTAL AGE AND MUTATIONThe Lancet, 1955