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Junichiro Machida

Showing results (11-20 of 21) with videos related to

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Human Genome Variation|July 21, 2021
Novel MSX1 frameshift mutation in a Japanese family with nonsyndromic oligodontiaJunya Adachi, Yoshihiko Aoki, Tadashi Tatematsu, et al.
Human Genome Variation|April 16, 2016
A novel PITX2 mutation causing iris hypoplasiaMasashi Kimura, Yoshihito Tokita, Junichiro Machida, et al.
Human Genome Variation|January 23, 2024
Novel frameshift variant of WNT10A in a Japanese patient with hypodontiaMichiyo Ando, Yoshihiko Aoki, Yasuto Sano, et al.
Human Molecular Genetics|February 6, 2015
A single nucleotide polymorphism associated with isolated cleft lip and palate, thyroid cancer and hypothyroidism alters the activity of an oral epithelium and thyroid enhancer near FOXE1Andrew C Lidral, Huan Liu, Steven A Bullard, et al.
Plos One|June 2, 2015
An aberrant splice acceptor site due to a novel intronic nucleotide substitution in MSX1 gene is the cause of congenital tooth agenesis in a Japanese familyTadashi Tatematsu, Masashi Kimura, Mitsuko Nakashima, et al.
Mutagenesis|July 30, 2015
Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patientAkio Shibata, Junichiro Machida, Seishi Yamaguchi, et al.
Human Genome Variation|July 21, 2021
A novel LRP6 variant in a Japanese family with oligodontiaHiroki Goto, Masashi Kimura, Junichiro Machida, et al.
Human Genome Variation|January 26, 2023
Novel WNT10A variant in a Japanese case of nonsyndromic oligodontiaJunya Adachi, Yoshihiko Aoki, Hiroto Izumi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 10, 2004
In a Vietnamese population, MSX1 variants contribute to cleft lip and palateYasushi Suzuki, Peter A Jezewski, Junichiro Machida, et al.
Human Molecular Genetics|September 26, 2009
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palateLina M Moreno, Maria Adela Mansilla, Steve A Bullard, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Human Genome Variation|July 21, 2021
Novel MSX1 frameshift mutation in a Japanese family with nonsyndromic oligodontiaJunya Adachi, Yoshihiko Aoki, Tadashi Tatematsu, et al.
Human Genome Variation|April 16, 2016
A novel PITX2 mutation causing iris hypoplasiaMasashi Kimura, Yoshihito Tokita, Junichiro Machida, et al.
Human Genome Variation|January 23, 2024
Novel frameshift variant of WNT10A in a Japanese patient with hypodontiaMichiyo Ando, Yoshihiko Aoki, Yasuto Sano, et al.
Human Molecular Genetics|February 6, 2015
A single nucleotide polymorphism associated with isolated cleft lip and palate, thyroid cancer and hypothyroidism alters the activity of an oral epithelium and thyroid enhancer near FOXE1Andrew C Lidral, Huan Liu, Steven A Bullard, et al.
Plos One|June 2, 2015
An aberrant splice acceptor site due to a novel intronic nucleotide substitution in MSX1 gene is the cause of congenital tooth agenesis in a Japanese familyTadashi Tatematsu, Masashi Kimura, Mitsuko Nakashima, et al.
Mutagenesis|July 30, 2015
Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patientAkio Shibata, Junichiro Machida, Seishi Yamaguchi, et al.
Human Genome Variation|July 21, 2021
A novel LRP6 variant in a Japanese family with oligodontiaHiroki Goto, Masashi Kimura, Junichiro Machida, et al.
Human Genome Variation|January 26, 2023
Novel WNT10A variant in a Japanese case of nonsyndromic oligodontiaJunya Adachi, Yoshihiko Aoki, Hiroto Izumi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 10, 2004
In a Vietnamese population, MSX1 variants contribute to cleft lip and palateYasushi Suzuki, Peter A Jezewski, Junichiro Machida, et al.
Human Molecular Genetics|September 26, 2009
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palateLina M Moreno, Maria Adela Mansilla, Steve A Bullard, et al.
Pageof 3