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You searched for: Author/Creator Hasegawa, Yuiko

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1. Blended phenotype of combination of HERC2 and AP3B2 deficiency and Angelman syndrome caused by paternal isodisomy of chromosome 15. Issue 10 (27th May 2021)

3. The novel and recurrent variants in exon 31 of CREBBP in Japanese patients with Menke–Hennekam syndrome. Issue 2 (15th October 2021)