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Journal of Human Genetics|April 29, 2016
Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type Ib in a patient with multilocus imprinting disturbance: a female-dominant phenomenon?Shinichiro Sano, Keiko Matsubara, Keisuke Nagasaki, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2016
Genome-wide multilocus imprinting disturbance analysis in Temple syndrome and Kagami-Ogata syndromeMasayo Kagami, Keiko Matsubara, Kazuhiko Nakabayashi, et al.Journal of Human Genetics|June 9, 2017
Maternally derived 15q11.2-q13.1 duplication and H19-DMR hypomethylation in a patient with Silver-Russell syndromeSumito Dateki, Masayo Kagami, Keiko Matsubara, et al.Bone|February 1, 2022
A novel deletion involving the first GNAS exon encoding Gsα causes PHP1A without methylation changes at exon A/BDevon Campbell, Monica Reyes, Sare Betul Kaygusuz, et al.Journal of Medical Genetics|February 19, 2018
A case of paternal uniparental isodisomy for chromosome 7 associated with overgrowthAkie Nakamura, Koji Muroya, Hiroko Ogata-Kawata, et al.Clinical Epigenetics|March 9, 2019
Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMRMasayo Kagami, Atsuhiro Yanagisawa, Miyuki Ota, et al.The Journal of Pediatrics|October 6, 2009
Maternal uniparental disomy 14 syndrome demonstrates prader-willi syndrome-like phenotypeKana Hosoki, Masayo Kagami, Touju Tanaka, et al.Genomics|February 10, 2009
Identification of the mouse paternally expressed imprinted gene Zdbf2 on chromosome 1 and its imprinted human homolog ZDBF2 on chromosome 2Hisato Kobayashi, Kaori Yamada, Shinnosuke Morita, et al.Clinical Epigenetics|April 8, 2021
Parthenogenetic mosaicism: generation via second polar body retention and unmasking of a likely causative PER2 variant for hypersomniaYohei Masunaga, Masayo Kagami, Fumiko Kato, et al.Clinical Epigenetics|July 1, 2021
Methylation status of genes escaping from X-chromosome inactivation in patients with X-chromosome rearrangementsSayaka Kawashima, Atsushi Hattori, Erina Suzuki, et al.Pageof 11