Yasuo Ueoka

Blepharophimosis sequence and <i>de novo</i> balanced autosomal translocation [46, XY,t(3;4)(q23;p15.2)]: Possible assignment of the trait to 3q23

Yoshimitsu Fukushima, Keiko Wakui, Toshiro Nishida et al. · American Journal of Medical Genetics · 1991 · 48 citations

Autosomal dominant familial exudative vitreoretinopathy in two Japanese families with<i>FZD4</i>mutations (H69Y and C181R)

Satoshi Omoto, Takaaki Hayashi, Kenji Kitahara et al. · Ophthalmic Genetics · 2004 · 42 citations

Four Japanese male patients with juvenile retinoschisis: Only three have mutations in the RS1 gene

Takaaki Hayashi, Satoshi Omoto, Tomokazu Takeuchi et al. · American Journal of Ophthalmology · 2004 · 23 citations

Juvenile Retinoschisis, Mendelian Disorder, Ophthalmology +5

Compound heterozygous <i>RDH5</i> mutations in familial fleck retina with night blindness

Takaaki Hayashi, Satoshi Goto‐Omoto, Tomokazu Takeuchi et al. · Acta Ophthalmologica Scandinavica · 2005 · 16 citations

Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization

Yoshimitsu Fukushima, J.M.N. Hoovers, M. Mannens et al. · Human Genetics · 1993 · 13 citations

Biology, Cryptic Paracentric Inversion, Natural Sciences +6