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Journal Abstract Search
222 related items for PubMed ID: 11770450
1. [Oto-mandibular dysplasias: genetics and nomenclature of syndromes]. Burglen L, Soupre V, Diner PA, Gonzalès M, Vazquez MP. Ann Chir Plast Esthet; 2001 Oct; 46(5):400-9. PubMed ID: 11770450 [Abstract] [Full Text] [Related]
2. [Morphological alterations of oto-mandibular syndromes]. Bettega G, Morand B, Lebeau J, Raphaël B. Ann Chir Plast Esthet; 2001 Oct; 46(5):495-506. PubMed ID: 11770456 [Abstract] [Full Text] [Related]
4. A family with dominant oculoauriculovertebral spectrum. Stoll C, Viville B, Treisser A, Gasser B. Am J Med Genet; 1998 Jul 24; 78(4):345-9. PubMed ID: 9714437 [Abstract] [Full Text] [Related]
5. Oculo-auriculo-vertebral spectrum: clinical and molecular analysis of 51 patients. Beleza-Meireles A, Hart R, Clayton-Smith J, Oliveira R, Reis CF, Venâncio M, Ramos F, Sá J, Ramos L, Cunha E, Pires LM, Carreira IM, Scholey R, Wright R, Urquhart JE, Briggs TA, Kerr B, Kingston H, Metcalfe K, Donnai D, Newman WG, Saraiva JM, Tassabehji M. Eur J Med Genet; 2015 Sep 24; 58(9):455-65. PubMed ID: 26206081 [Abstract] [Full Text] [Related]
7. Possible autosomal recessive inheritance in an infant with acrofacial dysostosis similar to Nager syndrome. Nur BG, Bernier FP, Oztekin O, Kardelen F, Kalay S, Parboosingh JS, Mihci E. Am J Med Genet A; 2013 Sep 24; 161A(9):2311-5. PubMed ID: 23913624 [Abstract] [Full Text] [Related]
8. Phenotypic and Molecular Heterogeneity in Mandibulofacial Dysostoses: A Case Series From India. Shenoy RD, Shetty V, Dheedene A, Menten B, Pandyanda Nanjappa D, Chakraborty G, Sips P, de Paepe A, Callewaert B, Chakraborty A. Cleft Palate Craniofac J; 2022 Nov 24; 59(11):1346-1351. PubMed ID: 34714179 [Abstract] [Full Text] [Related]
9. [Mandibulofacial dysostosis]. Moise C, Zaboş D. Oftalmologia; 1998 Nov 24; 45(4):81-3. PubMed ID: 10418634 [Abstract] [Full Text] [Related]
14. Autosomal recessive inheritance of Nager acrofacial dysostosis. Chemke J, Mogilner BM, Ben-Itzhak I, Zurkowski L, Ophir D. J Med Genet; 1988 Apr 24; 25(4):230-2. PubMed ID: 3367347 [Abstract] [Full Text] [Related]
15. Clinical and molecular delineation of mandibulofacial dysostosis with microcephaly in six Korean patients: When to consider EFTUD2 analysis? Ryu JH, Kim HY, Ko JM, Kim MJ, Seong MW, Choi BY, Chae JH. Eur J Med Genet; 2022 May 24; 65(5):104478. PubMed ID: 35395430 [Abstract] [Full Text] [Related]
16. The surgical management of Treacher Collins syndrome. Cobb AR, Green B, Gill D, Ayliffe P, Lloyd TW, Bulstrode N, Dunaway DJ. Br J Oral Maxillofac Surg; 2014 Sep 24; 52(7):581-9. PubMed ID: 24776174 [Abstract] [Full Text] [Related]
17. The pathogenesis of the Treacher Collins syndrome (mandibulofacial dysostosis). Poswillo D. Br J Oral Surg; 1975 Jul 24; 13(1):1-26. PubMed ID: 807232 [Abstract] [Full Text] [Related]
18. [Imaging of oto-mandibular dysplasias]. Montoya P, Leboucq N, Bigorre M. Ann Chir Plast Esthet; 2001 Oct 24; 46(5):424-46. PubMed ID: 11770452 [Abstract] [Full Text] [Related]
19. First and second branchial arch syndromes: multimodality approach. Senggen E, Laswed T, Meuwly JY, Maestre LA, Jaques B, Meuli R, Gudinchet F. Pediatr Radiol; 2011 May 24; 41(5):549-61. PubMed ID: 20924574 [Abstract] [Full Text] [Related]
20. [Treacher-Collins syndrome: clinical and genetic aspects apropos of 4 cases of which 1 is familial]. Chaabouni M, Fersi M, Belghith N, Maazoul F, M'rad R, Ben Jemaa L, Gandoura N, Chaabouni H. Tunis Med; 2007 Oct 24; 85(10):885-90. PubMed ID: 18236814 [Abstract] [Full Text] [Related] Page: [Next] [New Search]