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Journal Abstract Search
392 related items for PubMed ID: 9409870
1. 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]
2. Agenesis of corpus callosum in three sibs. Naritomi K, Chinen Y, Asato Y. Jpn J Hum Genet; 1997 Dec 12; 42(4):539-41. PubMed ID: 9560954 [No Abstract] [Full Text] [Related]
4. [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]
6. 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]
13. Callosal defect, microcephaly, severe mental retardation, and other anomalies in three sibs. da-Silva EO. Am J Med Genet; 1988 Apr 27; 29(4):837-43. PubMed ID: 3400727 [Abstract] [Full Text] [Related]
14. Acrocallosal syndrome: new findings. Moeschler JB, Pober BR, Holmes LB, Graham JM. Am J Med Genet; 1989 Mar 27; 32(3):306-10. PubMed ID: 2729349 [Abstract] [Full Text] [Related]