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.
25. Auditory canal atresia, humeroscapular synostosis, and other skeletal abnormalities: confirmation of the autosomal recessive "SAMS" syndrome. ter Heide H; Bulstra SK; Reekers A; Schrander JJ; Schrander-Stumpel CT Am J Med Genet; 2002 Jul; 110(4):359-64. PubMed ID: 12116210 [TBL] [Abstract][Full Text] [Related]
26. [Bone malformations associated with deletion of the long arm of chromosome X]. Hurgoiu V; Suciu S; Nicoară Z; Florescu P; David-Mark S Rev Pediatr Obstet Ginecol Pediatr; 1988; 37(4):373-6. PubMed ID: 3150606 [No Abstract] [Full Text] [Related]
27. [Skeletal anomalies of the hand, skull, and spine in a group of 15 children with Turner's syndrome]. Kuklík M; Klán Z; Holík F Cesk Pediatr; 1980 Oct; 35(10):529-31. PubMed ID: 7438264 [No Abstract] [Full Text] [Related]
28. [Case of Rubinstein-Taybi syndrome]. Tartara R Minerva Pediatr; 1973 Mar; 25(8):326-8. PubMed ID: 4716245 [No Abstract] [Full Text] [Related]
29. [Goltz syndrome. Presentation of 2 cases]. Pascual-Castroviejo I; Luengo dos Santos A; Baguero Paret G An Esp Pediatr; 1982 Jun; 16(6):524-6. PubMed ID: 7125405 [No Abstract] [Full Text] [Related]
30. [Weill-Marchesani syndrome. Apropos of a case]. Bebe M Ann Pediatr (Paris); 1983 Nov; 30(9):673-7. PubMed ID: 6419665 [No Abstract] [Full Text] [Related]
31. Distinctive syndrome of short stature, craniosynostosis, skeletal changes, and malformed ears. Hurst JA; Winter RM; Baraitser M Am J Med Genet; 1988 Jan; 29(1):107-15. PubMed ID: 3344763 [TBL] [Abstract][Full Text] [Related]
32. [A new case of mucopolysaccharidosis type VII with major skeletal abnormalities]. Capdeville R; Boissinot G; Graveleau D; Maroteaux P Ann Pediatr (Paris); 1983 Nov; 30(9):689-92. PubMed ID: 6229213 [No Abstract] [Full Text] [Related]
33. Velo-facio-skeletal syndrome versus Aarskog syndrome. Fryns JP; Devriendt K Am J Med Genet; 1996 Sep; 64(4):604. PubMed ID: 8870930 [No Abstract] [Full Text] [Related]
34. [Clinical and anthropological studies of Rubinstein-Taybi syndrome]. Rett A; Kahlich-Koenner DM; Madl W Wien Med Wochenschr; 1969 May; 119(19):378-83. PubMed ID: 5783074 [No Abstract] [Full Text] [Related]
37. Elaboration of the phenotypic changes of the upper limbs in the Neu-Laxova syndrome. Shved IA; Lazjuk GI; Cherstvoy ED Am J Med Genet; 1985 Jan; 20(1):1-11. PubMed ID: 3970062 [TBL] [Abstract][Full Text] [Related]
38. [The Roberts-SC phocomelia syndrome. Apropos of a case without cytogenetic changes and review of the literature]. López-Herce J; Rodríguez Sánchez C; Duelo M; Fontoura M; González M; Gracia R; Oliver A; Peralta A An Esp Pediatr; 1985 Dec; 23(8):588-92. PubMed ID: 3006564 [No Abstract] [Full Text] [Related]
39. [Diagnosis and treatment of gastrointestinal bleeding in Bean syndrome]. Bottero A; Benedetti L; Sasson L; Baylez M; Cordisco MR; Rubio M; Nastri M; Ruiz JA Acta Gastroenterol Latinoam; 2008 Dec; 38(4):278-83. PubMed ID: 19157383 [TBL] [Abstract][Full Text] [Related]
40. [Infantile encephalopathies and complex dysmorphies. A case of Rubinstein-Taybi syndrome]. Arnould G; Laxenaire M; Picard L; Andre JM; Brichet B Rev Otoneuroophtalmol; 1970; 42(6):306-12. PubMed ID: 5502128 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]