Yasuhiro Kido

Koshigaya, Japan

Last Updated: 09/26/2026

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Found 11 publications

Divergent variant patterns among 19 patients with Rubinstein-Taybi syndrome uncovered by comprehensive genetic analysis including whole genome sequencing.

Divergent variant patterns among 19 patients with Rubinstein-Taybi syndrome uncovered by comprehensive genetic analysis including whole genome sequencing.

Journal: Clinical genetics

Published: November 04, 2021

Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases.

Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases.

Journal: Human mutation

Published: July 30, 2021

Current status of non-invasive prenatal testing in Japan.

Current status of non-invasive prenatal testing in Japan.

Journal: The journal of obstetrics and gynaecology research

Published: December 26, 2016

Chromosomal abnormalities in 1354 Japanese patients with azoospermia due to spermatogenic dysfunction.

Chromosomal abnormalities in 1354 Japanese patients with azoospermia due to spermatogenic dysfunction.

Journal: International journal of urology : official journal of the Japanese Urological Association

Published: December 02, 2015

Differing phenotypes of Moyamoya disease in a familial case involving heterozygous c.14429G > A variant in RNF213.

Differing phenotypes of Moyamoya disease in a familial case involving heterozygous c.14429G > A variant in RNF213.

Journal: Pediatrics international : official journal of the Japan Pediatric Society

Published: November 20, 2014

Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation.

Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation.

Journal: Molecular cytogenetics

Published: June 11, 2014

Additional patients with 4q deletion: Severe growth delay and polycystic kidney disease associated with 4q21q22 loss.

Additional patients with 4q deletion: Severe growth delay and polycystic kidney disease associated with 4q21q22 loss.

Journal: Pediatrics international : official journal of the Japan Pediatric Society

Published: May 01, 2014

QOL in caregivers of Japanese patients with Prader-Willi syndrome with reference to age and genotype.

QOL in caregivers of Japanese patients with Prader-Willi syndrome with reference to age and genotype.

Journal: American journal of medical genetics. Part A

Published: December 26, 2013

Autism spectrum disorders and hyperactive/impulsive behaviors in Japanese patients with Prader-Willi syndrome: a comparison between maternal uniparental disomy and deletion cases.

Autism spectrum disorders and hyperactive/impulsive behaviors in Japanese patients with Prader-Willi syndrome: a comparison between maternal uniparental disomy and deletion cases.

Journal: American journal of medical genetics. Part A

Published: November 07, 2013

Further characterization of atypical features in auriculocondylar syndrome caused by recessive PLCB4 mutations.

Further characterization of atypical features in auriculocondylar syndrome caused by recessive PLCB4 mutations.

Journal: American journal of medical genetics. Part A

Published: February 19, 2013

Testosterone replacement therapy to improve secondary sexual characteristics and body composition without adverse behavioral problems in adult male patients with Prader-Willi syndrome: an observational study.

Testosterone replacement therapy to improve secondary sexual characteristics and body composition without adverse behavioral problems in adult male patients with Prader-Willi syndrome: an observational study.

Journal: American journal of medical genetics. Part A

Published: April 07, 2012

Showing 1-11 of 11

Last Updated: 09/26/2026