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Journal Abstract Search
93 related items for PubMed ID: 23264967
21. Adams-Oliver Syndrome - Follow-up of a Large Scalp Defect. Lorenz L, Sönnichsen K, Müller-Hansen I, Poets C. Klin Padiatr; 2014 Jul; 226(4):250-1. PubMed ID: 24515817 [No Abstract] [Full Text] [Related]
22. The recognition of bilateral craniofacial deformities. Glass D. Trans Br Soc Study Orthod; 2014 Jul; 5(6):105-16. PubMed ID: 5290221 [No Abstract] [Full Text] [Related]
23. [Adams-Oliver syndrome]. Bayou F, Boussofara L, Bennani ZL, Ghariani N, Saïdi W, Belajouza C, Denguezli M, Nouira R. Ann Dermatol Venereol; 2011 Oct; 138(10):712-4. PubMed ID: 21978514 [No Abstract] [Full Text] [Related]
24. Adams-Oliver Syndrome: Limited Expression. Kasinathan A, Sharawat IK, Das G, Sankhyan N. Indian J Pediatr; 2019 Jan; 86(1):101-102. PubMed ID: 29948730 [No Abstract] [Full Text] [Related]
25. Adams-Oliver syndrome in a newborn infant. Zakanj Z, Bedek D, Kotrulja L, Ozanic Bulic S. Int J Dermatol; 2016 Feb; 55(2):215-7. PubMed ID: 24697559 [No Abstract] [Full Text] [Related]
30. [The Adams-Oliver syndrome. A case report]. Yéo S, Perrot P, Bellier-Waast F, David A, Duteille F. Chir Main; 2010 Sep; 29(4):274-6. PubMed ID: 20727808 [Abstract] [Full Text] [Related]
31. Rescue of neurodegeneration in the Fig4 null mouse by a catalytically inactive FIG4 transgene. Lenk GM, Frei CM, Miller AC, Wallen RC, Mironova YA, Giger RJ, Meisler MH. Hum Mol Genet; 2016 Jan 15; 25(2):340-7. PubMed ID: 26604144 [Abstract] [Full Text] [Related]
36. Ectrodactary, ectodermal dysplasia, and cleft lip-palate syndrome. Choong YY, Norazlina B. Med J Malaysia; 2001 Mar 15; 56(1):88-91. PubMed ID: 11503303 [Abstract] [Full Text] [Related]
37. [The Adams-Oliver syndrome in Spain: the epidemiological aspects]. Martínez-Frías ML, Arroyo Carrera I, Muñoz-Delgado NJ, Nieto Conde C, Rodríguez-Pinilla E, Urioste Azcorra M, Omeñaca Teres F, García Alix A. An Esp Pediatr; 1996 Jul 15; 45(1):57-61. PubMed ID: 8849132 [Abstract] [Full Text] [Related]
40. A de novo heterozygous point mutation in the p63 gene causing the syndrome of ectrodactyly, ectodermal dysplasia and facial clefting. Pozo G, Canún S, Kofman-Alfaro S, Zenteno JC. Br J Dermatol; 2004 Oct 15; 151(4):930-2. PubMed ID: 15491445 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]