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Journal Abstract Search

84 related items for PubMed ID: 9560954

  • 1. Agenesis of corpus callosum in three sibs.
    Naritomi K, Chinen Y, Asato Y.
    Jpn J Hum Genet; 1997 Dec; 42(4):539-41. PubMed ID: 9560954
    [No Abstract] [Full Text] [Related]

  • 2. Possible new autosomal recessive syndrome of partial agenesis of the corpus callosum, pontine hypoplasia, focal white matter changes, hypotonia, mental retardation, and minor anomalies.
    Jonas RE, Kimonis VE, Morales A.
    Am J Med Genet; 1997 Dec 12; 73(2):184-8. PubMed ID: 9409870
    [Abstract] [Full Text] [Related]

  • 3. New autosomal recessive multiple congenital abnormalities/mental retardation syndrome with craniofacial dysmorphism absent corpus callosum, iris colobomas and connective tissue dysplasia.
    Temtamy SA, Salam MA, Aboul-Ezz EH, Hussein HA, Helmy SA, Shalash BA.
    Clin Dysmorphol; 1996 Jul 12; 5(3):231-40. PubMed ID: 8818452
    [Abstract] [Full Text] [Related]

  • 4. MRI of the brain in the Cohen syndrome: a relatively large corpus callosum in patients with mental retardation and microcephaly.
    Kivitie-Kallio S, Autti T, Salonen O, Norio R.
    Neuropediatrics; 1998 Dec 12; 29(6):298-301. PubMed ID: 10029348
    [Abstract] [Full Text] [Related]

  • 5. Callosal defect, microcephaly, severe mental retardation, and other anomalies in three sibs.
    da-Silva EO.
    Am J Med Genet; 1988 Apr 12; 29(4):837-43. PubMed ID: 3400727
    [Abstract] [Full Text] [Related]

  • 6. Corpus callosum agenesis in Coffin-Lowry syndrome.
    Soekarman D, Fryns JP.
    Genet Couns; 1994 Apr 12; 5(1):77-80. PubMed ID: 8031540
    [Abstract] [Full Text] [Related]

  • 7. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
    Camera G, Centa A, Pozzolo S, Camera A.
    Clin Dysmorphol; 1993 Oct 12; 2(4):317-21. PubMed ID: 8305962
    [Abstract] [Full Text] [Related]

  • 8. Spectrum of corpus callosum agenesis.
    Sztriha L.
    Pediatr Neurol; 2005 Feb 12; 32(2):94-101. PubMed ID: 15664768
    [Abstract] [Full Text] [Related]

  • 9. [Familial agenesis of the corpus callosum: a new form].
    Castro-Gago M, Rodriguez-Nuñez A, Eiris J, Peña J, Tojo R, Novo-Rodriguez I.
    Arch Fr Pediatr; 1993 Apr 12; 50(4):327-30. PubMed ID: 8379821
    [Abstract] [Full Text] [Related]

  • 10. Corpus callosum agenesis, facial anomalies, Robin sequence, and other anomalies: a new autosomal recessive syndrome?
    Toriello HV, Carey JC.
    Am J Med Genet; 1988 Sep 12; 31(1):17-23. PubMed ID: 3223497
    [Abstract] [Full Text] [Related]

  • 11. Japanese kindred with FG syndrome.
    Kato R, Niikawa N, Nagai T, Fukushima Y.
    Am J Med Genet; 1994 Aug 15; 52(2):242-3. PubMed ID: 7802020
    [No Abstract] [Full Text] [Related]

  • 12. Delineation of the da-Silva syndrome.
    Naritomi K, Tohma T, Goya Y, Shiroma N, Hirayama K.
    Am J Med Genet; 1994 Feb 01; 49(3):313-6. PubMed ID: 8209892
    [Abstract] [Full Text] [Related]

  • 13. Agenesis of the corpus callosum: clinical and genetic study in 63 young patients.
    Bedeschi MF, Bonaglia MC, Grasso R, Pellegri A, Garghentino RR, Battaglia MA, Panarisi AM, Di Rocco M, Balottin U, Bresolin N, Bassi MT, Borgatti R.
    Pediatr Neurol; 2006 Mar 01; 34(3):186-93. PubMed ID: 16504787
    [Abstract] [Full Text] [Related]

  • 14. Craniosynostosis, agenesis of the corpus callosum, serve mental retardation, distinctive facies, camptodactyly, and hypogonadism.
    Lin AE, Gettig E.
    Am J Med Genet; 1990 Apr 01; 35(4):582-5. PubMed ID: 2333890
    [No Abstract] [Full Text] [Related]

  • 15. Occurrence of Andermann syndrome out of French Canada--agenesis of the corpus callosum with neuronopathy.
    Battistella PA.
    Neuropediatrics; 1993 Aug 01; 24(4):239. PubMed ID: 8232787
    [No Abstract] [Full Text] [Related]

  • 16. 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 Aug 01; 14(3):343-8. PubMed ID: 14577680
    [Abstract] [Full Text] [Related]

  • 17. [Associated brain anomalies and clinical findings in corpus callosum dysgenesis].
    Alkan A, Kutlu R, Baysal T, Siğirci A, Altinok T, Orkan I, Hallaç T, Saraç K.
    Tani Girisim Radyol; 2003 Dec 01; 9(4):411-7. PubMed ID: 14730948
    [Abstract] [Full Text] [Related]

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  • 19. [Agenesis of the corpus callosum].
    Nielsen LH.
    Ugeskr Laeger; 1995 Feb 06; 157(6):737-9. PubMed ID: 7701633
    [Abstract] [Full Text] [Related]

  • 20. Greig cephalopolysyndactyly syndrome with dysgenesis of the corpus callosum in a Bedouin family.
    Marafie MJ, Temtamy SA, Rajaram U, al-Awadi SA, el-Badramany MH, Farag TI.
    Am J Med Genet; 1996 Dec 18; 66(3):261-4. PubMed ID: 8985483
    [Abstract] [Full Text] [Related]

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