HARADA Naoki | Kyushu Medical Science

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著作論文

Mirror duplication of chromosome 21 with complete phenotype of Down syndrome.
Genotype-phenotype correlation of 5p- syndrome : pitfall of diagnosis
Monozygotic Twins with Discordant Sexual Phenotypes due to Different Rations of Mosaicism of 47, X, idic(Y), idic(Y)/46, X, idic(Y)/45, X
Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid
Less Frequent NSD1-Intragenic Deletions in Japanese Sotos Syndrome: Analysis of 30 Patients by NSD1-Exon Array CGH, Quantitative Fluorescent Duplex PCR, and Fluorescence In Situ Hybridization
Complete hydatidiform mole and normal live birth following intracytoplasmic sperm injection
Duplication (22)(q11.22-q11.23) without coloboma and cleft lip or palate
Miller syndrome with novel dihydroorotate dehydrogenase gene mutations
Prenatal findings in a fetus with contiguous gene syndrome caused by deletion of Xp22.3 that includes locus for X-linked recessive type of chondrodysplasia punctata (CDPX1)

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