11 results on '"Kuwajima, Katsuko"'
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2. A pediatric case of critical illness polyneuropathy: clinical and pathological findings
3. Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms
4. An AciI polymorphism in the 3′ untranslated region of the human phosphomannomutase 2 (PMM2) gene
5. Missense mutations in the phosphomannomutase 2 gene of two Japanese siblings with carbohydrate-deficient glycoprotein syndrome type I
6. Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms
7. Brachmann-de Lange syndrome and congenital heart disease
8. Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation
9. Weaver syndrome in two Japanese children
10. Diagnostic hand anomalies in Smith-Magenis syndrome: Four new patients with del (17)(p11.2p11.2)
11. Lipoma of the Corpus callosum: Report of a Case and Review of the Literature.
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