Shinsuke Ninomiya

Isolation of a Testis-Specific cDNA on Chromosome 17q from a Region Adjacent to the Breakpoint of t(12, 17) Observed in a Patient with Acampomelic Campomelic Dysplasia and Sex Reversal

Shinsuke Ninomiya, Minoru Isomura, Kouji Narahara et al. · Human Molecular Genetics · 1996 · 50 citations · Full text

Autosomal dominant congenital cataract and microphthalmia associated with a familial t(2;16) translocation

Yuji Yokoyama, Kouji Narahara, Kazushiro Tsuji et al. · Human Genetics · 1992 · 45 citations

Ocular Disease, Familial T, Ophthalmology +5

Growth hormone deficiency and empty sella syndrome in a boy with dup(x)(q13.3→q21.2)

Yuji Yokoyama, Kouji Narahara, Kazushiro Tsuji et al. · American Journal of Medical Genetics · 1992 · 44 citations

Renal and skin involvement in a patient with complete Kearns‐Sayre syndrome

Kazuhiro Mori, Kouji Narahara, Shinsuke Ninomiya et al. · American Journal of Medical Genetics · 1991 · 40 citations

Two novel mutations of SURF1 in Leigh syndrome with cytochrome c oxidase deficiency

Michio Teraoka, Yuji Yokoyama, Shinsuke Ninomiya et al. · Human Genetics · 1999 · 37 citations

Mendelian Disorder, Biochemistry, Genetic Disorder +9