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Journal of Human Genetics
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June 2, 2017
A commentary on ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin-Siris-like syndrome
Tadashi Kaname, Kumiko Yanagi
Nihon Yakurigaku Zasshi. Folia Pharmacologica Japonica
|
July 2, 2025
[Mechanism of pathogenesis by a gain-of-function variant of STAT6 causing severe allergic diseases and potential for development of molecularly targeted drugs]
Kumiko Yanagi, Tadashi Kaname
Journal of Human Genetics
|
February 7, 2014
A commentary on the promise of whole-exome sequencing in medical genetics
Tadashi Kaname, Kumiko Yanagi, Kenji Naritomi
Journal of Human Genetics
|
November 30, 2012
A commentary on the diagnostic utility of exome sequencing in Joubert syndrome and related disorders
Tadashi Kaname, Kumiko Yanagi, Kenji Naritomi
American Journal of Medical Genetics. Part A
|
October 21, 2024
Clinical Features of a Japanese Girl With Radio-Tartaglia Syndrome due to a SPEN Truncating Variant
Eriko Nishi, Kumiko Yanagi, Nobuhiko Okamoto, et al.
Congenital Anomalies
|
August 26, 2004
Novel alternative splicing of human faciogenital dysplasia 1 gene
Kumiko Yanagi, Tadashi Kaname, Yasutsugu Chinen, et al.
Brain & Development
|
November 29, 2018
A novel mutation in the GATAD2B gene associated with severe intellectual disability
Kimiko Ueda, Kumiko Yanagi, Tadashi Kaname, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
June 30, 2022
Feeding disorder in a patient with Wiedemann-Steiner syndrome
Hiroyuki Iijima, Kumiko Yanagi, Tadashi Kaname, et al.
American Journal of Medical Genetics. Part A
|
May 12, 2006
Neurobehavioral disorders in patients with Aarskog-Scott syndrome affected by novel FGD1 mutations
Tadashi Kaname, Kumiko Yanagi, Nobuhiko Okamoto, et al.
Molecular Genetics & Genomic Medicine
|
February 14, 2024
Clinical details of individuals with Rauch-Steindl syndrome due to NSD2 truncating variants
Eriko Nishi, Kumiko Yanagi, Tadashi Kaname, et al.
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of 10
Search research articles
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Showing results (1-10 of 93) with videos related to
Sort By:
Page
of 10
Journal of Human Genetics
|
June 2, 2017
A commentary on ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin-Siris-like syndrome
Tadashi Kaname, Kumiko Yanagi
Nihon Yakurigaku Zasshi. Folia Pharmacologica Japonica
|
July 2, 2025
[Mechanism of pathogenesis by a gain-of-function variant of STAT6 causing severe allergic diseases and potential for development of molecularly targeted drugs]
Kumiko Yanagi, Tadashi Kaname
Journal of Human Genetics
|
February 7, 2014
A commentary on the promise of whole-exome sequencing in medical genetics
Tadashi Kaname, Kumiko Yanagi, Kenji Naritomi
Journal of Human Genetics
|
November 30, 2012
A commentary on the diagnostic utility of exome sequencing in Joubert syndrome and related disorders
Tadashi Kaname, Kumiko Yanagi, Kenji Naritomi
American Journal of Medical Genetics. Part A
|
October 21, 2024
Clinical Features of a Japanese Girl With Radio-Tartaglia Syndrome due to a SPEN Truncating Variant
Eriko Nishi, Kumiko Yanagi, Nobuhiko Okamoto, et al.
Congenital Anomalies
|
August 26, 2004
Novel alternative splicing of human faciogenital dysplasia 1 gene
Kumiko Yanagi, Tadashi Kaname, Yasutsugu Chinen, et al.
Brain & Development
|
November 29, 2018
A novel mutation in the GATAD2B gene associated with severe intellectual disability
Kimiko Ueda, Kumiko Yanagi, Tadashi Kaname, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
June 30, 2022
Feeding disorder in a patient with Wiedemann-Steiner syndrome
Hiroyuki Iijima, Kumiko Yanagi, Tadashi Kaname, et al.
American Journal of Medical Genetics. Part A
|
May 12, 2006
Neurobehavioral disorders in patients with Aarskog-Scott syndrome affected by novel FGD1 mutations
Tadashi Kaname, Kumiko Yanagi, Nobuhiko Okamoto, et al.
Molecular Genetics & Genomic Medicine
|
February 14, 2024
Clinical details of individuals with Rauch-Steindl syndrome due to NSD2 truncating variants
Eriko Nishi, Kumiko Yanagi, Tadashi Kaname, et al.
Page
of 10