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Journal Abstract Search

392 related items for PubMed ID: 9409870

  • 41. Two siblings with midline field defects and Hirschsprung disease: variable expression of Toriello-Carey or new syndrome?
    Jespers A, Buntinx I, Melis K, Vaerenberg M, Janssens G.
    Am J Med Genet; 1993 Aug 15; 47(2):299-302. PubMed ID: 8213924
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  • 42. Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES syndrome): a newly recognized autosomal recessive syndrome.
    Kantaputra PN, Kunachaichote J, Patikulsila P.
    Am J Med Genet; 2001 Nov 01; 103(4):283-8. PubMed ID: 11746007
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  • 43. Ullrich-Turner syndrome with agenesis of the corpus callosum.
    Kimura M, Nakajima M, Yoshino K.
    Am J Med Genet; 1990 Oct 01; 37(2):227-8. PubMed ID: 2248289
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  • 44. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A, Hoyme HE, Dallapiccola B, Zackai E, Hudgins L, McDonald-McGinn D, Bahi-Buisson N, Romano C, Williams CA, Brailey LL, Zuberi SM, Carey JC.
    Pediatrics; 2008 Feb 01; 121(2):404-10. PubMed ID: 18245432
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  • 45. Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndrome.
    Schinzel A, Schmid W.
    Am J Med Genet; 1980 Feb 01; 6(3):241-9. PubMed ID: 7424976
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  • 46. A new case of neonatal progeroid syndrome with agenesis of corpus callosum.
    Abdel-Salam GM, Czeizel AE.
    Genet Couns; 1999 Feb 01; 10(4):377-81. PubMed ID: 10631926
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  • 47. Toriello-Carey syndrome: report of a new case.
    Camera G, Righi E, Romagnoli G.
    Clin Dysmorphol; 1993 Jul 01; 2(3):260-3. PubMed ID: 7506967
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  • 48. Two siblings with a new Aicardi-Goutières-like syndrome.
    Schwarz KB, Ferrie CD, Woods CG.
    Dev Med Child Neurol; 2002 Jun 01; 44(6):422-5. PubMed ID: 12088311
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  • 49. Acrocallosal syndrome: additional manifestations.
    Casamassima AC, Beneck D, Gewitz MH, Horowitz MA, Woolf PK, Pettersen IM, Shapiro LR.
    Am J Med Genet; 1989 Mar 01; 32(3):311-7. PubMed ID: 2658584
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  • 50. A Turkish case of subcortical/subependymal heterotopia associated with corpus callosum dysgenesis, craniofacial dysmorphism, severe eye abnormalities, and growth-mental retardation.
    Caksen H, Tuncer O, Ataş B, Demirok A, Unal O, Ikbal M, Odabaş D.
    Genet Couns; 2003 Mar 01; 14(3):343-8. PubMed ID: 14577680
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  • 53. The neurofaciodigitorenal (NFDR) syndrome.
    Freire-Maia N, Pinheiro M, Opitz JM.
    Am J Med Genet; 1982 Mar 01; 11(3):329-36. PubMed ID: 7081297
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  • 54. The neurology of carbonic anhydrase type II deficiency syndrome.
    Bosley TM, Salih MA, Alorainy IA, Islam MZ, Oystreck DT, Suliman OS, al Malki S, Suhaibani AH, Khiari H, Beckers S, van Wesenbeeck L, Perdu B, AlDrees A, Elmalik SA, Van Hul W, Abu-Amero KK.
    Brain; 2011 Dec 01; 134(Pt 12):3502-15. PubMed ID: 22120147
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  • 56. [Agenesis of the corpus callosum].
    Nielsen LH.
    Ugeskr Laeger; 1995 Feb 06; 157(6):737-9. PubMed ID: 7701633
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  • 57. Central nervous system abnormalities in Kabuki (Niikawa-Kuroki) syndrome.
    Mihçi E, Taçoy S, Haspolat S, Karaali K.
    Am J Med Genet; 2002 Sep 01; 111(4):448-9. PubMed ID: 12210310
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