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Journal Abstract Search
131 related items for PubMed ID: 6859092
41. Craniotelencephalic dysplasia in sisters: further delineation of a possible syndrome. Hughes HE, Harwood-Nash DC, Becker LE. Am J Med Genet; 1983 Mar; 14(3):557-65. PubMed ID: 6859106 [Abstract] [Full Text] [Related]
42. [Cerebro-hepato-renal (Zellweger) syndrome]. Szabó L, Garzuly F, Kádas L. Orv Hetil; 1974 Nov 10; 115(45):2681-4. PubMed ID: 4419167 [No Abstract] [Full Text] [Related]
43. Polycystic kidneys and liver in two siblings with other severe congenital abnormalities. Tan KL, Thomas MA. Med J Malaya; 1970 Sep 10; 25(1):46-9. PubMed ID: 4249495 [No Abstract] [Full Text] [Related]
44. Editorial comment: variability in the Smith-Lemli-Opitz syndrome: overlap with the Meckel syndrome. Lowry RB. Am J Med Genet; 1983 Mar 10; 14(3):429-33. PubMed ID: 6859094 [No Abstract] [Full Text] [Related]
45. A new case of megalencephaly and perisylvian polymicrogyria with post-axial polydactyly and hydrocephalus: MPPH syndrome. Colombani M, Chouchane M, Pitelet G, Morales L, Callier P, Pinard JP, Lion-François L, Thauvin-Robinet C, Mugneret F, Huet F, Guibaud L, Faivre L. Eur J Med Genet; 2006 Mar 10; 49(6):466-71. PubMed ID: 16807158 [Abstract] [Full Text] [Related]
46. Unusual association of cerebral and renal abnormalities. Winter RM, Wigglesworth JS. Clin Dysmorphol; 1993 Jan 10; 2(1):71-5. PubMed ID: 8298742 [Abstract] [Full Text] [Related]
47. Trisomy 18 with multiple rare malformations: report of one case. Su PH, Chen JY, Hsu CH, Chen SJ, Chan SW, Lin LL. Acta Paediatr Taiwan; 2007 Jan 10; 48(5):272-5. PubMed ID: 18254577 [Abstract] [Full Text] [Related]
49. Meckel-Gruber syndrome. Gazioğlu N, Vural M, Seçkin MS, Tüysüz B, Akpir E, Kuday C, Ilikkan B, Erginel A, Cenani A. Childs Nerv Syst; 1998 Mar 10; 14(3):142-5. PubMed ID: 9579873 [Abstract] [Full Text] [Related]
50. 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]
52. Meckel syndrome in different populations. Lurie IW, Prytkov AN, Meldere LV. Am J Med Genet; 1984 Aug 10; 18(4):661-9. PubMed ID: 6486166 [Abstract] [Full Text] [Related]
53. Intrachromosomal triplication of 2q11.2-q21 in a severely malformed infant: case report and review of triplications and their possible mechanism. Wang J, Reddy KS, Wang E, Halderman L, Morgan BL, Lachman RS, Lin HJ, Cornford ME. Am J Med Genet; 1999 Feb 12; 82(4):312-7. PubMed ID: 10051164 [Abstract] [Full Text] [Related]
55. The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24. Paavola P, Salonen R, Weissenbach J, Peltonen L. Nat Genet; 1995 Oct 12; 11(2):213-5. PubMed ID: 7550354 [Abstract] [Full Text] [Related]
56. Diprosopus with associated malformations: report of two cases. Pavone L, Camera G, Grasso S, Gambini C, Barberis M, Garaffo S, Russo S. Am J Med Genet; 1987 Sep 12; 28(1):85-8. PubMed ID: 3674120 [Abstract] [Full Text] [Related]
57. A mouse model for Meckel syndrome type 3. Cook SA, Collin GB, Bronson RT, Naggert JK, Liu DP, Akeson EC, Davisson MT. J Am Soc Nephrol; 2009 Apr 12; 20(4):753-64. PubMed ID: 19211713 [Abstract] [Full Text] [Related]
59. Fibrosis of the liver in Meckel Gruber syndrome. de Silva MV, Senanayake HM. Indian Pediatr; 2001 Nov 12; 38(11):1325-7. PubMed ID: 11721082 [No Abstract] [Full Text] [Related]