Hiroshi Yoshihashi

Phenotypic spectrum of CHARGE syndrome with CHD7 mutations

Michihiko Aramaki, Toru Udaka, Rika Kosaki et al. · The Journal of Pediatrics · 2006 · 165 citations

Mendelian Disorder, Genetic Disorder, Genetics +5

Imprinting of Human GRB10 and Its Mutations in Two Patients with Russell-Silver Syndrome

Hiroshi Yoshihashi, Katsuhiro Maeyama, Rika Kosaki et al. · The American Journal of Human Genetics · 2000 · 91 citations · Full text

Genetic Disorder, Medicine, Genetics +7

Characterization of the aryl hydrocarbon receptor repressor gene and association of its Pro185Ala polymorphism with micropenis

Hideki Fujita, Rika Kosaki, Hiroshi Yoshihashi et al. · Teratology · 2002 · 48 citations · Full text

The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss

Rika Yasukawa, Hideaki Moteki, Shin‐ya Nishio et al. · Genes · 2019 · 45 citations · Full text

Further delineation of 9q22 deletion syndrome associated with basal cell nevus (Gorlin) syndrome: Report of two cases and review of the literature

Kayono Yamamoto, Hiroshi Yoshihashi, Noritaka Furuya et al. · Congenital Anomalies · 2009 · 34 citations