These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
167 related articles for article (PubMed ID: 11694546)
41. Clinical and genetic heterogeneity in frontometaphyseal dysplasia: severe progressive scoliosis in two families. Morava E; Illés T; Weisenbach J; Kárteszi J; Kosztolányi G Am J Med Genet A; 2003 Jan; 116A(3):272-7. PubMed ID: 12503106 [TBL] [Abstract][Full Text] [Related]
42. Confirmation of the Catania brachydactylous type of acrofacial dysostosis: report of a second family. Wulfsberg EA; Campbell AB; Lurie IW; Eanet KR Am J Med Genet; 1996 Jun; 63(4):554-7. PubMed ID: 8826434 [TBL] [Abstract][Full Text] [Related]
43. Novel mutations in geleophysic dysplasia type 1. Porayette P; Fruitman D; Lauzon JL; Le Goff C; Cormier-Daire V; Sanders SP; Pinto-Rojas A; Perez-Atayde AR Pediatr Dev Pathol; 2014; 17(3):209-16. PubMed ID: 24251637 [TBL] [Abstract][Full Text] [Related]
44. Diagnostic criteria, clinical characteristics, and natural history of Cohen syndrome. Chandler KE; Kidd A; Al-Gazali L; Kolehmainen J; Lehesjoki AE; Black GC; Clayton-Smith J J Med Genet; 2003 Apr; 40(4):233-41. PubMed ID: 12676892 [TBL] [Abstract][Full Text] [Related]
45. The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype. Tekin M; Kavaz A; Berberoğlu M; Fitoz S; Ekim M; Ocal G; Akar N Am J Med Genet A; 2004 Oct; 130A(3):284-7. PubMed ID: 15378538 [TBL] [Abstract][Full Text] [Related]