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Journal Abstract Search

84 related items for PubMed ID: 9560954

  • 21. An intragenic deletion of the NFIA gene in a patient with a hypoplastic corpus callosum, craniofacial abnormalities and urinary tract defects.
    Rao A, O'Donnell S, Bain N, Meldrum C, Shorter D, Goel H.
    Eur J Med Genet; 2014 Feb; 57(2-3):65-70. PubMed ID: 24462883
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  • 22. Toriello-Carey syndrome in a patient with a de novo balanced translocation [46,XY,t(2;14)(q33;q22)] interrupting SATB2.
    Tegay DH, Chan KK, Leung L, Wang C, Burkett S, Stone G, Stanyon R, Toriello HV, Hatchwell E.
    Clin Genet; 2009 Mar; 75(3):259-64. PubMed ID: 19170718
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  • 23. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
    Elia M, Striano P, Fichera M, Gaggero R, Castiglia L, Galesi O, Malacarne M, Pierluigi M, Amato C, Musumeci SA, Romano C, Majore S, Grammatico P, Zara F, Striano S, Faravelli F.
    Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647
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  • 24. Acrocallosal syndrome: additional manifestations.
    Casamassima AC, Beneck D, Gewitz MH, Horowitz MA, Woolf PK, Pettersen IM, Shapiro LR.
    Am J Med Genet; 1989 Mar; 32(3):311-7. PubMed ID: 2658584
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  • 25. Acrocallosal syndrome: new findings.
    Moeschler JB, Pober BR, Holmes LB, Graham JM.
    Am J Med Genet; 1989 Mar; 32(3):306-10. PubMed ID: 2729349
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  • 26. [Agenesis of the corpus callosum in 2 brothers].
    Dogan K, Dogan S, Lovrencić M.
    Lijec Vjesn; 1967 Mar; 89(5):377-85. PubMed ID: 6063234
    [No Abstract] [Full Text] [Related]

  • 27. Agenesis of the corpus callosum in a mother and son.
    Inbar D, Halpern GJ, Weitz R, Sadeh M, Shohat M.
    Am J Med Genet; 1997 Mar 17; 69(2):152-4. PubMed ID: 9056551
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  • 31. Triplets with growth failure, microcephaly, mental retardation, nail hypoplasia and corpus callosum agenesis: is it a variant of Coffin-Siris or a new syndrome?
    Kirel B, Kural N, Yakut A, Adapinar B.
    Turk J Pediatr; 2000 Mar 17; 42(2):171-6. PubMed ID: 10936989
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  • 32. Bilateral sensorineural deafness, partial agenesis of the corpus callosum, and arachnoid cysts in two sisters.
    Hendriks YM, Laan LA, Vielvoye GJ, van Haeringen A.
    Am J Med Genet; 1999 Sep 10; 86(2):183-6. PubMed ID: 10449658
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  • 34. Hypogenitalism in the acrocallosal syndrome.
    Temtamy SA, Meguid NA.
    Am J Med Genet; 1989 Mar 10; 32(3):301-5. PubMed ID: 2658583
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  • 35. Ullrich-Turner syndrome with agenesis of the corpus callosum.
    Kimura M, Nakajima M, Yoshino K.
    Am J Med Genet; 1990 Oct 10; 37(2):227-8. PubMed ID: 2248289
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  • 36. Clinical and behavioral characteristics in FG syndrome.
    Graham JM, Superneau D, Rogers RC, Corning K, Schwartz CE, Dykens EM.
    Am J Med Genet; 1999 Aug 27; 85(5):470-5. PubMed ID: 10405444
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  • 40. Unusual presentation of gastroesophageal reflux with corpus callosum agenesis, cleft palate and mental retardation.
    Desai BN, Joshi SM, Malik S, Mittal S, Dandge VP.
    Indian Pediatr; 1991 Nov 27; 28(11):1328-30. PubMed ID: 1808058
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