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Journal Abstract Search
91 related items for PubMed ID: 842092
1. [The oto-palato-digital syndrome (Taybi) (author's transl)]. Szabó L, Perjés K, Mangliár K. Z Orthop Ihre Grenzgeb; 1977 Feb; 115(1):75-82. PubMed ID: 842092 [Abstract] [Full Text] [Related]
3. Oto-palato-digital syndrome with features of type I and II in brothers. Horn D, Nitz I, Bollmann R. Genet Couns; 1995 Feb; 6(3):233-40. PubMed ID: 8588852 [Abstract] [Full Text] [Related]
6. On the phenotypic overlap between "severe" oto-palato digital type II syndrome and Larsen syndrome. Variable manifestation of a single autosomal dominant gene. Alembik Y, Stoll C, Messer J. Genet Couns; 1997 Feb; 8(2):133-7. PubMed ID: 9219012 [Abstract] [Full Text] [Related]
7. Fountain syndrome: further delineation of the clinical syndrome and follow-up data. Van Buggenhout GJ, Van Ravenswaaij-Arts CM, Renier WO, Van de Wiel MP, Trommelen JC, Pijkels E, Hamel BC, Fryns JP. Genet Couns; 1996 Feb; 7(3):177-86. PubMed ID: 8897038 [Abstract] [Full Text] [Related]
8. [A case of dwarfism with oto-palato-digital involvement (author's transl)]. Farriaux JP, Dubois O, Maroteaux P, Fontaine G. J Radiol Electrol Med Nucl; 1974 Feb; 55(2):137-42. PubMed ID: 4408413 [No Abstract] [Full Text] [Related]
9. The oto-palato-digital (OPD) syndrome in females. Gorlin RJ, Poznanski AK, Hendon I. Oral Surg Oral Med Oral Pathol; 1973 Feb; 35(2):218-24. PubMed ID: 4513067 [No Abstract] [Full Text] [Related]
10. [Oto-palato-digital syndrome. Report of a case in a female]. Sirvent Gómez J, Rodríguez Valcárcel G, Alfayate Miguélez S, Pombo Felipe F. An Esp Pediatr; 1984 Jun; 20(9):905-10. PubMed ID: 6486585 [No Abstract] [Full Text] [Related]
11. [The Rubinstein-Taybi syndrome (author's transl)]. Theile U, Draf U, Heldt JP. Dtsch Med Wochenschr; 1978 Sep 29; 103(39):1505-10. PubMed ID: 688891 [Abstract] [Full Text] [Related]
12. [Rubinstein-Taybi-syndrome of probably monocygotic twins and 3 other children (author's transl)]. Buchinger G, Ströder J. Klin Padiatr; 1973 Jul 29; 185(4):296-307. PubMed ID: 4795800 [No Abstract] [Full Text] [Related]
13. Familial transmission of a dysmorphic syndrome: a variant example of Kabuki syndrome? Belengeanu V, Rozsnyai K, Farcaş S, Velea I, Fryns JP. Genet Couns; 2005 Jul 29; 16(2):167-71. PubMed ID: 16080297 [Abstract] [Full Text] [Related]
19. A familial syndrome with micrognathia, cleft palate, short neck and stature, vertebral anomalies and mental retardation. Mathieu M, De Broca A, Bony H, Piussan C. Genet Couns; 1993 Sep 01; 4(4):299-303. PubMed ID: 8110419 [Abstract] [Full Text] [Related]
20. Oto-palato-digital syndrome in an Iranian infant. Farhud DD, Walizadeh GR, Farhud I. Monatsschr Kinderheilkd; 1989 Oct 01; 137(10):681-3. PubMed ID: 2555708 [Abstract] [Full Text] [Related] Page: [Next] [New Search]