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Journal of human genetics

Showing results (71-80 of 3,698) with videos related to

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Journal of Human Genetics|March 4, 2018
RNF213-related susceptibility of Japanese CADASIL patients to intracranial arterial stenosisWing Tung Esther Yeung, Ikuko Mizuta, Akiko Watanabe-Hosomi, et al.
Journal of Human Genetics|February 17, 2018
Self-perceptions from people with Down syndrome in JapanMio Wakai, Rina Takahashi, Satomi Higashigawa, et al.
Journal of Human Genetics|December 22, 2017
Focal facial dermal dysplasia type 4: identification of novel CYP26C1 mutations in unrelated patientsBeom Hee Lee, Fanny Morice-Picard, Franck Boralevi, et al.
Journal of Human Genetics|February 15, 2018
A homozygous NOP14 variant is likely to cause recurrent pregnancy lossToshifumi Suzuki, Mahdiyeh Behnam, Firooze Ronasian, et al.
Journal of Human Genetics|December 24, 2017
GAREM1 regulates the PR interval on electrocardiogramsHye Ok Kim, Ji Eun Lim, Myung Jun Kim, et al.
Journal of Human Genetics|December 14, 2017
Characteristic dysmorphic features in congenital disorders of glycosylation type IIbYoon-Myung Kim, Go Hun Seo, Euiseok Jung, et al.
Journal of Human Genetics|July 15, 2016
Block-based association tests for rare variants using Kullback-Leibler divergenceDegang Zhu, Yue-Qing Hu, Shili Lin
Journal of Human Genetics|November 1, 2006
Alpha-adrenoceptor gene variants and autonomic nervous system function in a young healthy Japanese populationTetsuro Matsunaga, Koichiro Yasuda, Tetsuya Adachi, et al.
Journal of Human Genetics|November 8, 2006
Different roles of MTHFR C677T and A1298C polymorphisms in colorectal adenoma and colorectal cancer: a meta-analysisYan Huang, Shizhong Han, Yao Li, et al.
Journal of Human Genetics|November 8, 2006
MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndromeMei-Rong Li, Hong Pan, Xin-Hua Bao, et al.
Pageof 370

Showing results (71-80 of 3,698) with videos related to

Sort By:
Pageof 370
Journal of Human Genetics|March 4, 2018
RNF213-related susceptibility of Japanese CADASIL patients to intracranial arterial stenosisWing Tung Esther Yeung, Ikuko Mizuta, Akiko Watanabe-Hosomi, et al.
Journal of Human Genetics|February 17, 2018
Self-perceptions from people with Down syndrome in JapanMio Wakai, Rina Takahashi, Satomi Higashigawa, et al.
Journal of Human Genetics|December 22, 2017
Focal facial dermal dysplasia type 4: identification of novel CYP26C1 mutations in unrelated patientsBeom Hee Lee, Fanny Morice-Picard, Franck Boralevi, et al.
Journal of Human Genetics|February 15, 2018
A homozygous NOP14 variant is likely to cause recurrent pregnancy lossToshifumi Suzuki, Mahdiyeh Behnam, Firooze Ronasian, et al.
Journal of Human Genetics|December 24, 2017
GAREM1 regulates the PR interval on electrocardiogramsHye Ok Kim, Ji Eun Lim, Myung Jun Kim, et al.
Journal of Human Genetics|December 14, 2017
Characteristic dysmorphic features in congenital disorders of glycosylation type IIbYoon-Myung Kim, Go Hun Seo, Euiseok Jung, et al.
Journal of Human Genetics|July 15, 2016
Block-based association tests for rare variants using Kullback-Leibler divergenceDegang Zhu, Yue-Qing Hu, Shili Lin
Journal of Human Genetics|November 1, 2006
Alpha-adrenoceptor gene variants and autonomic nervous system function in a young healthy Japanese populationTetsuro Matsunaga, Koichiro Yasuda, Tetsuya Adachi, et al.
Journal of Human Genetics|November 8, 2006
Different roles of MTHFR C677T and A1298C polymorphisms in colorectal adenoma and colorectal cancer: a meta-analysisYan Huang, Shizhong Han, Yao Li, et al.
Journal of Human Genetics|November 8, 2006
MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndromeMei-Rong Li, Hong Pan, Xin-Hua Bao, et al.
Pageof 370