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[文献書誌] Silao,CL,Shirakawa,T,Nishiyama,K,Padilla,C and Matsuo,M.: "Molecular basis of glucose-6-phosphate dehydrogenase deficiency among"Filipinos Pediatr Int. 41. 138-141 (1999)
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[文献書誌] Laosombat,V,Dissaneevate,S,Peerapittayamongkol,C and Matsuo,M.: "Neonatal hyperbilirubinemia associated with Southeast Asian ovalocytosis"Am J Hematol. 60. 136-139 (1999)
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[文献書誌] Kosho,T,Muroya,K,Nagai,T,Fujimoto,M,Yokoya,S,Sakamoto,H,Hirano,T,Terasaki,H,Ohashi,H,Nishimura,G,Sato,S,Matsuo,N and Ogata,T.: "Skeletal features and growth patterns in 14 patients with haploinsufficiency of SHOX: implications for the development of Turner syndrome"J Clin Endocrinol Metab. 84. 4613-4621 (1999)
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[文献書誌] Nishimura,G,Ikegawa,S,Saga,T,Nagai,T,Aya,M and Kawano,T.: "Metaphyseal anadysplasia: evidence of genetic heterogeneity"Am J Med Genet. 82. 43-48 (1999)
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[文献書誌] Kantaputra,PN,Gorlin,RJ,Ukarapol,N,Unachak,K and Sudasna,J.: "Robinow (fetal face) syndrome: report of a boy with dominant type and an infant with recessive type"Am J Med Genet. 84. 1-7 (1999)
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[文献書誌] Simizu,Y,Ao,H,Soemantri,A,Tiwawech,D,Settheetham-Ishida,W,Kayame,OW,Kimura,M,Nishioka,T and Ishida,T.: "Sero-and molecular-typing of duffy blood group in Southest Asians and Oceanians; demontration of cryptic genotypes by the PCR-zRELP study"Human Biology. 72(in press). (2000)