Petty syndrome and Fontaine-Farriaux syndrome: Delineation of a single syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33468/fullpdf
Reference14 articles.
1. Braddock SR Golabi M Hall BD 2008 Petty syndrome: Further delineation of a rare “old” syndrome. Presented at the 29th David W. Smith Workshop on Malformations and Morphogenesis
2. Fontaine-Farriaux syndrome: A recognizable craniosynostosis syndrome with nail, skeletal, abdominal, and central nervous system anomalies;Castori;Am J Med Genet Part A,2009
3. Petty-Laxova-Wiedemann progeroid syndrome: Further phenotypical delineation and confirmation of a rare syndrome of premature aging;Delgado-Luengo;Am J Med Genet Part A,2009
4. Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome;Eriksson;Nature,2003
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2. A 9-year-old Korean girl with Fontaine progeroid syndrome: a case report with further phenotypical delineation and description of clinical course during long-term follow-up;BMC Medical Genetics;2019-11-27
3. Premature Ageing Syndromes;Harper's Textbook of Pediatric Dermatology;2019-11-20
4. De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise;The American Journal of Human Genetics;2017-11
5. Fetal Progeria: Prenatal Sonographic Findings in Petty Syndrome;J ULTRAS MED;2013
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