Two sisters resembling Gorlin-Chaudhry-Moss syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference8 articles.
1. Petty syndrome and Fontaine-Farriaux syndrome: Delineation of a single syndrome;Braddock;Am J Med Genet Part A,2010
2. An etiologic and nosologic overview of craniosynostosis syndromes;Cohen;Birth Defects,1975
3. Craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies-A new syndrome?;Gorlin;J Pediatr,1960
4. Large scalp and skull defect in patient with aplasia cutis congenital;Henriques;Arq Neuropsiquiatr,2004
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3. A rare male patient with Fontaine progeroid syndrome caused by p.R217H de novo mutation in SLC25A24;American Journal of Medical Genetics Part A;2018-10-17
4. De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction;The American Journal of Human Genetics;2017-11
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