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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Disease and HDAC8[original query]
Expression of the class 1 histone deacetylases HDAC8 and 3 are associated with improved survival of patients with metastatic melanoma.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2015 Jul 28 (7): 884-94.
Wilmott James S, Colebatch Andrew J, Kakavand Hojabr, Shang Ping, Carlino Matteo S, Thompson John F, Long Georgina V, Scolyer Richard A, Hersey Pet
Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies.
Genetics in medicine : official journal of the American College of Medical Genetics 2018 8 21 (3): 663-675.
Yuan Bo, Neira Juanita, Pehlivan Davut, Santiago-Sim Teresa, Song Xiaofei, Rosenfeld Jill, Posey Jennifer E, Patel Vipulkumar, Jin Weihong, Adam Margaret P, Baple Emma L, Dean John, Fong Chin-To, Hickey Scott E, Hudgins Louanne, Leon Eyby, Madan-Khetarpal Suneeta, Rawlins Lettie, Rustad Cecilie F, Stray-Pedersen Asbjørg, Tveten Kristian, Wenger Olivia, Diaz Jullianne, Jenkins Laura, Martin Laura, McGuire Marianne, Pietryga Marguerite, Ramsdell Linda, Slattery Leah, , Abid Farida, Bertuch Alison A, Grange Dorothy, Immken LaDonna, Schaaf Christian P, Van Esch Hilde, Bi Weimin, Cheung Sau Wai, Breman Amy M, Smith Janice L, Shaw Chad, Crosby Andrew H, Eng Christine, Yang Yaping, Lupski James R, Xiao Rui, Liu Pengf
[Analysis of clinical manifestation and genetic mutations in two patients with Cornelia de Lange syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018 8 35 (4): 493-497.
Miao Yequan, Zhu Yueyue, Zhang Qigang, Guo Haowei, Zhao Yuxiang, Cheng Longfei, Han Liangrong, Ning Ying, Pan Qio
Rare copy number variants contribute pathogenic alleles in patients with intestinal malrotation.
Molecular genetics & genomic medicine 2019 Jan e549.
Salehi Karlslätt Karin, Pettersson Maria, Jäntti Nina, Szafranski Przemyslaw, Wester Tomas, Husberg Britt, Ullberg Ulla, Stankiewicz Pawel, Nordgren Ann, Lundin Johanna, Lindstrand Anna, Nordenskjöld Agne
[Genetic variant analysis of a neonate with Cornelia de Lange syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 3 37 (4): 449-451.
Sun Yuanyuan, Chen Cuie, Di Tianwei, Shao Haoran, Zhu Ronghe, Zhu Yanke, Zhou Aihua, Wang Q
Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families. GWAS Catalog
Genes 2021 May 12 (5): .
Al-Sarraj Yasser, Al-Dous Eman, Taha Rowaida Z, Ahram Dina, Alshaban Fouad, Tolfat Mohammed, El-Shanti Hatem, Albagha Omar M
Genetic diagnosis of fetal microcephaly at a single tertiary center in China.
Frontiers in genetics 2023 5 14 1112153.
You Wang, Fang Fu, Tingying Lei, Li Zhen, Qiong Deng, Hang Zhou, Chunling Ma, Ken Cheng, Ruibin Huang, Ru Li, Qiuxia Yu, Lushan Li, Jin Han, Xin Yang, Dongzhi Li, Can Li
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