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Hidehito Inagaki

Showing results (81-90 of 98) with videos related to

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Placenta|October 19, 2025
Possible involvement of a ZC3H4 gene splicing defect in the etiology of pre-eclampsiaHikari Yoshizawa, Hidehito Inagaki, Rei Yoshimoto, et al.
Molecular Cytogenetics|May 4, 2017
A case with concurrent duplication, triplication, and uniparental isodisomy at 1q42.12-qter supporting microhomology-mediated break-induced replication model for replicative rearrangementsTomohiro Kohmoto, Nana Okamoto, Takuya Naruto, et al.
European Journal of Human Genetics : EJHG|February 25, 2010
Paternal origin of the de novo constitutional t(11;22)(q23;q11)Tamae Ohye, Hidehito Inagaki, Hiroshi Kogo, et al.
Journal of Human Genetics|April 8, 2016
A PDE3A mutation in familial hypertension and brachydactyly syndromeHiroko Boda, Hidetoshi Uchida, Nobue Takaiso, et al.
BMC Research Notes|June 10, 2015
PCSK5 mutation in a patient with the VACTERL associationYukio Nakamura, Shingo Kikugawa, Shoji Seki, et al.
BMC Medical Genetics|October 28, 2015
Intragenic duplication in the PKHD1 gene in autosomal recessive polycystic kidney diseaseJun Miyazaki, Mayuko Ito, Haruki Nishizawa, et al.
Molecular Cytogenetics|December 6, 2014
Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocationDivya Mishra, Takema Kato, Hidehito Inagaki, et al.
Prenatal Diagnosis|February 17, 2023
Clinical application of long-read nanopore sequencing in a preimplantation genetic testing pre-clinical workup to identify the junction for complex Xq chromosome rearrangement-related diseaseTasuku Mariya, Yui Shichiri, Takeshi Sugimoto, et al.
Human Genetics|August 24, 2023
Breakpoints in complex chromosomal rearrangements correspond to transposase-accessible regions of DNA from mature spermTakeshi Sugimoto, Hidehito Inagaki, Tasuku Mariya, et al.
Journal of Human Genetics|August 26, 2017
Corrigendum: Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndromeMiwako Nagasaka, Mariko Taniguchi-Ikeda, Hidehito Inagaki, et al.
Pageof 10

Showing results (81-90 of 98) with videos related to

Sort By:
Pageof 10
Placenta|October 19, 2025
Possible involvement of a ZC3H4 gene splicing defect in the etiology of pre-eclampsiaHikari Yoshizawa, Hidehito Inagaki, Rei Yoshimoto, et al.
Molecular Cytogenetics|May 4, 2017
A case with concurrent duplication, triplication, and uniparental isodisomy at 1q42.12-qter supporting microhomology-mediated break-induced replication model for replicative rearrangementsTomohiro Kohmoto, Nana Okamoto, Takuya Naruto, et al.
European Journal of Human Genetics : EJHG|February 25, 2010
Paternal origin of the de novo constitutional t(11;22)(q23;q11)Tamae Ohye, Hidehito Inagaki, Hiroshi Kogo, et al.
Journal of Human Genetics|April 8, 2016
A PDE3A mutation in familial hypertension and brachydactyly syndromeHiroko Boda, Hidetoshi Uchida, Nobue Takaiso, et al.
BMC Research Notes|June 10, 2015
PCSK5 mutation in a patient with the VACTERL associationYukio Nakamura, Shingo Kikugawa, Shoji Seki, et al.
BMC Medical Genetics|October 28, 2015
Intragenic duplication in the PKHD1 gene in autosomal recessive polycystic kidney diseaseJun Miyazaki, Mayuko Ito, Haruki Nishizawa, et al.
Molecular Cytogenetics|December 6, 2014
Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocationDivya Mishra, Takema Kato, Hidehito Inagaki, et al.
Prenatal Diagnosis|February 17, 2023
Clinical application of long-read nanopore sequencing in a preimplantation genetic testing pre-clinical workup to identify the junction for complex Xq chromosome rearrangement-related diseaseTasuku Mariya, Yui Shichiri, Takeshi Sugimoto, et al.
Human Genetics|August 24, 2023
Breakpoints in complex chromosomal rearrangements correspond to transposase-accessible regions of DNA from mature spermTakeshi Sugimoto, Hidehito Inagaki, Tasuku Mariya, et al.
Journal of Human Genetics|August 26, 2017
Corrigendum: Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndromeMiwako Nagasaka, Mariko Taniguchi-Ikeda, Hidehito Inagaki, et al.
Pageof 10