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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 - 4 (of 4 Records)

Query Trace: Disease and EHMT1[original query]
De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.
PLoS genetics 2016 Apr 12 (4): e1005963.
Priest James R, Osoegawa Kazutoyo, Mohammed Nebil, Nanda Vivek, Kundu Ramendra, Schultz Kathleen, Lammer Edward J, Girirajan Santhosh, Scheetz Todd, Waggott Daryl, Haddad Francois, Reddy Sushma, Bernstein Daniel, Burns Trudy, Steimle Jeffrey D, Yang Xinan H, Moskowitz Ivan P, Hurles Matthew, Lifton Richard P, Nickerson Debbie, Bamshad Michael, Eichler Evan E, Mital Seema, Sheffield Val, Quertermous Thomas, Gelb Bruce D, Portman Michael, Ashley Euan
Eight novel susceptibility loci and putative causal variants in atopic dermatitis. GWAS Catalog
The Journal of allergy and clinical immunology 2021 Jun .
Tanaka Nao, Koido Masaru, Suzuki Akari, Otomo Nao, Suetsugu Hiroyuki, Kochi Yuta, Tomizuka Kouhei, Momozawa Yukihide, Kamatani Yoichiro, , Ikegawa Shiro, Yamamoto Kazuhiko, Terao Chikas
[Genetic analysis of three patients with Kleefstra syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 4 38 (4): 347-350.
Gong Yuhong, Zhu Xiaoming, Li Wen, Dong Guizhen, Xu Biao, Zhao Hongli
Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development.
Human genetics 2022 11 .
Safizadeh Shabestari Seyed Ali, Nassir Nasna, Sopariwala Samana, Karimov Islam, Tambi Richa, Zehra Binte, Kosaji Noor, Akter Hosneara, Berdiev Bakhrom K, Uddin Mohamm
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