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International Journal of Cancer
|
July 2, 2009
Genome-wide DNA methylation profiles in liver tissue at the precancerous stage and in hepatocellular carcinoma
Eri Arai, Saori Ushijima, Masahiro Gotoh, et al.
Journal of Human Genetics
|
March 8, 2003
Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan
Mingshun Li, Kinya Ishikawa, Shuta Toru, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
September 8, 2005
Genetic classification of lung adenocarcinoma based on array-based comparative genomic hybridization analysis: its association with clinicopathologic features
Tatsuhiro Shibata, Satomi Uryu, Akiko Kokubu, et al.
Cancer Science
|
January 20, 2007
Genome-wide array-based comparative genomic hybridization analysis of pancreatic adenocarcinoma: identification of genetic indicators that predict patient outcome
Panayiotis Loukopoulos, Tatsuhiro Shibata, Hiroto Katoh, 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 rearrangements
Tomohiro Kohmoto, Nana Okamoto, Takuya Naruto, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2007
Partial tandem duplication of GRIA3 in a male with mental retardation
Tomohiro Chiyonobu, Shin Hayashi, Kazuhiro Kobayashi, et al.
American Journal of Medical Genetics. Part A
|
January 18, 2018
A rare male patient with classic Rett syndrome caused by MeCP2_e1 mutation
Narumi Tokaji, Hiromichi Ito, Tomohiro Kohmoto, et al.
Cancer Science
|
September 25, 2009
Genome-wide DNA methylation profiles in urothelial carcinomas and urothelia at the precancerous stage
Naotaka Nishiyama, Eri Arai, Yoshitomo Chihara, et al.
American Journal of Medical Genetics. Part A
|
November 3, 2007
22q13 Microduplication in two patients with common clinical manifestations: a recognizable syndrome?
Nobuhiko Okamoto, Takeo Kubota, Yutaka Nakamura, et al.
Human Genome Variation
|
July 23, 2020
Molecular diagnosis of an infant with <i>TSC2</i>/<i>PKD1</i> contiguous gene syndrome
Keita Osumi, Kenichi Suga, Akemi Ono, et al.
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of 25
Search research articles
Search
Showing results (171-180 of 241) with videos related to
Sort By:
Page
of 25
International Journal of Cancer
|
July 2, 2009
Genome-wide DNA methylation profiles in liver tissue at the precancerous stage and in hepatocellular carcinoma
Eri Arai, Saori Ushijima, Masahiro Gotoh, et al.
Journal of Human Genetics
|
March 8, 2003
Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan
Mingshun Li, Kinya Ishikawa, Shuta Toru, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
September 8, 2005
Genetic classification of lung adenocarcinoma based on array-based comparative genomic hybridization analysis: its association with clinicopathologic features
Tatsuhiro Shibata, Satomi Uryu, Akiko Kokubu, et al.
Cancer Science
|
January 20, 2007
Genome-wide array-based comparative genomic hybridization analysis of pancreatic adenocarcinoma: identification of genetic indicators that predict patient outcome
Panayiotis Loukopoulos, Tatsuhiro Shibata, Hiroto Katoh, 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 rearrangements
Tomohiro Kohmoto, Nana Okamoto, Takuya Naruto, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2007
Partial tandem duplication of GRIA3 in a male with mental retardation
Tomohiro Chiyonobu, Shin Hayashi, Kazuhiro Kobayashi, et al.
American Journal of Medical Genetics. Part A
|
January 18, 2018
A rare male patient with classic Rett syndrome caused by MeCP2_e1 mutation
Narumi Tokaji, Hiromichi Ito, Tomohiro Kohmoto, et al.
Cancer Science
|
September 25, 2009
Genome-wide DNA methylation profiles in urothelial carcinomas and urothelia at the precancerous stage
Naotaka Nishiyama, Eri Arai, Yoshitomo Chihara, et al.
American Journal of Medical Genetics. Part A
|
November 3, 2007
22q13 Microduplication in two patients with common clinical manifestations: a recognizable syndrome?
Nobuhiko Okamoto, Takeo Kubota, Yutaka Nakamura, et al.
Human Genome Variation
|
July 23, 2020
Molecular diagnosis of an infant with <i>TSC2</i>/<i>PKD1</i> contiguous gene syndrome
Keita Osumi, Kenichi Suga, Akemi Ono, et al.
Page
of 25