Gorlin-Chaudhry-Moss or Saethre-Chotzen syndrome?
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1995.tb04309.x/fullpdf
Reference13 articles.
1. The mapping of a gene for craniosynostosis: evidence for linkage of Saethre-Chotzen syndrome to distal chromosome 7p;Brueton;J Med Genet,1992
2. Saethre-Chotzen syndrome with trigonocephaly;Cristofori;Am J Med Genet,1992
3. On the classification of acrocephalosyndactyly syndromes;Escobar;Clin Genet,1977
4. Craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora. dental and eye anomalies - a new syndrome;Gorlin;J Pediatr,1960
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1. De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction;The American Journal of Human Genetics;2017-11
2. Hereditary premature closure of a coronal suture in the Abraham Lincoln family;Gene;2013-10
3. Gorlin-chaudhry-moss syndrome revisited: Expanding the phenotype;American Journal of Medical Genetics Part A;2013-05-17
4. Necrotizing soft tissue infection of the scalp after fronto-facial advancement by internal distraction in a 7-year old girl with Gorlin–Chaudhry–Moss syndrome – A case report;Journal of Cranio-Maxillofacial Surgery;2011-12
5. Two sisters resembling Gorlin-Chaudhry-Moss syndrome;American Journal of Medical Genetics Part A;2011-09-09
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