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Journal Abstract Search
724 related items for PubMed ID: 8779326
21. Duplication of (2)(q11.1-q13.2) in a boy with mental retardation and cleft lip and palate: another clefting gene locus on proximal 2q? Riegel M, Schinzel A. Am J Med Genet; 2002 Jul 22; 111(1):76-80. PubMed ID: 12124740 [Abstract] [Full Text] [Related]
22. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies. Hamel BC, Mariman EC, van Beersum SE, Schoonbrood-Lenssen AM, Ropers HH. Am J Med Genet; 1994 Jul 15; 51(4):591-7. PubMed ID: 7943045 [Abstract] [Full Text] [Related]
23. PHAVER syndrome: an autosomal recessive syndrome of limb pterygia, congenital heart anomalies, vertebral defects, ear anomalies, and radial defects. Powell CM, Chandra RS, Saal HM. Am J Med Genet; 1993 Nov 01; 47(6):807-11. PubMed ID: 8279476 [Abstract] [Full Text] [Related]
24. Multiple congenital malformations in two sibs reminiscent of hydrolethalus and pseudotrisomy 13 syndromes. Dincsoy MY, Salih MA, al-Jurayyan N, al Saadi M, Patel PJ. Am J Med Genet; 1995 Apr 10; 56(3):317-21. PubMed ID: 7778599 [Abstract] [Full Text] [Related]
26. New syndrome in three affected siblings. Crane JP, Heise RL. Pediatrics; 1981 Aug 10; 68(2):235-7. PubMed ID: 7267231 [Abstract] [Full Text] [Related]
27. Walker-Warburg syndrome with cleft lip and cleft palate in two sibs. Burton BK, Dillard RG, Weaver RG. Am J Med Genet; 1987 Jul 10; 27(3):537-41. PubMed ID: 3631127 [Abstract] [Full Text] [Related]
28. Congenital heart defect in a patient with deletion of chromosome 7q. Tiller GE, Watson MS, Duncan LM, Dowton SB. Am J Med Genet; 1988 Feb 10; 29(2):283-7. PubMed ID: 3354600 [Abstract] [Full Text] [Related]
29. A syndrome of severe midface retraction, multiple skull anomalies, clubfeet, and cardiac and renal malformations in sibs. Schinzel A, Giedion A. Am J Med Genet; 1978 Feb 10; 1(4):361-75. PubMed ID: 665725 [Abstract] [Full Text] [Related]
32. Bilateral renal agenesis with Potter phenotype, cleft palate, anomalies of the cardiovascular system, skeletal anomalies including hexadactyly and bifid metacarpal. A new syndrome? Holzgreve W, Wagner H, Rehder H. Am J Med Genet; 1984 May 10; 18(1):177-82. PubMed ID: 6741992 [No Abstract] [Full Text] [Related]
34. Cleft lip and palate, corneal opacities and profound psychomotor retardation. A newly recognized genetic syndrome? Anyane-Yeboa K, Mackay C, Taterka P, Merkrebs A, Allendorf D. Cleft Palate J; 1983 Jul 10; 20(3):246-50. PubMed ID: 6577987 [Abstract] [Full Text] [Related]
35. [3 children with velocardiofacial (Shprintzen) syndrome]. Lie DA, Beemer FA. Ned Tijdschr Geneeskd; 1996 Feb 17; 140(7):372-5. PubMed ID: 8628424 [Abstract] [Full Text] [Related]
36. The Gardner-Silengo-Wachtel or genito-palato-cardiac syndrome: male pseudohermaphroditism with micrognathia, cleft palate, and conotruncal cardiac defect. Greenberg F, Gresik MV, Carpenter RJ, Law SW, Hoffman LP, Ledbetter DH. Am J Med Genet; 1987 Jan 17; 26(1):59-64. PubMed ID: 3812578 [Abstract] [Full Text] [Related]
37. Familial holoprosencephaly, heart defects, and polydactyly. Hennekam RC, van Noort G, de la Fuente AA. Am J Med Genet; 1991 Nov 01; 41(2):258-62. PubMed ID: 1785646 [Abstract] [Full Text] [Related]
39. Oral-facial-digital (OFD) syndrome with associated features: a new syndrome or genetic heterogeneity and variability? Morán-Barroso V, Valdés Flores M, García-Cavazos R, Kofman-Alfaro S, Saavedra-Ontiveros D. Clin Dysmorphol; 1998 Jan 01; 7(1):55-7. PubMed ID: 9546832 [Abstract] [Full Text] [Related]