Hirohito Shima

4PUBLICATIONS
17CO-AUTHORS
Genetics not elsewhere classifiedEpigenetics (incl. genome methylation and epigenomics)Other psychology not elsewhere classifiedDevelopmental genetics (incl. sex determination)
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Publications (4)

|Jul 11, 2025
De Novo Splice Site Variant of TCF12 in a Boy With Isolated Kallmann Syndrome.

Erina Suzuki, Hirohito Shima, Aki Ueda

|May 07, 2024
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities.

Satoshi Narumi, Keisuke Nagasaki, Mitsuo Kiriya

|Apr 29, 2024
A case of 49,XXXYY followed-up from infancy to adulthood with review of literature.

Junko Kanno, Akinobu Miura, Sayaka Kawashima

|Jun 07, 2021
SOX10 Mutation Screening for 117 Patients with Kallmann Syndrome.

Hirohito Shima, Etsuro Tokuhiro, Shingo Okamoto

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