Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: ARMC4[original query] |
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Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia. The European respiratory journal 2014 Dec 44 (6): 1579-88. Raidt Johanna, Wallmeier Julia, Hjeij Rim, Onnebrink Jörg Große, Pennekamp Petra, Loges Niki T, Olbrich Heike, Häffner Karsten, Dougherty Gerard W, Omran Heymut, Werner Claudi |
Discovery of Aberrant Alteration of Genome in Colorectal Cancer by Exome Sequencing. The American journal of the medical sciences 2019 8 358 (5): 340-349. Liang Yuanzi, Jiang Liejun, Zhong Xiaogang, Hochwald Steven N, Wang Yongsi, Huang Lihe, Nie Qiumiao, Huang Huayi, Xu Jun- |
Rare homozygosity in amyotrophic lateral sclerosis suggests the contribution of recessive variants to disease genetics. Journal of the neurological sciences 2019 May 402 62-68. Goldstein Orly, Kedmi Merav, Gana-Weisz Mali, Twito Shir, Nefussy Beatrice, Vainer Batel, Fainmesser Yaara, Abraham Alon, Nayshool Omri, Orr-Urtreger Avi, Drory Vivian |
Genotype and phenotype evaluation of patients with primary ciliary dyskinesia: First results from Turkey. Pediatric pulmonology 2019 11 55 (2): 383-393. Emiralio?lu Nagehan, Ta?k?ran Ekim Z, Ko?ukcu Can, Bilgiç Elif, Atilla Pergin, Kaya Bengisu, Günayd?n Önder, Yüzba??o?lu Ay?e, Tu?cu Gökçen Dil?a, Ademhan Dilber, Ery?lmaz Polat Sanem, Gharibzadeh H?zal Mina, Yalç?n Ebru, Do?ru Deniz, Kiper Nural, Alika?ifo?lu Mehmet, Özçelik U? |
The Relationship between Genotype and Phenotype in Primary Ciliary Dyskinesia Patients. Sisli Etfal Hastanesi tip bulteni 2021 55 (2): 188-192. Kilinc Ayse Ayzit, Cebi Memnune Nur, Ocak Zeynep, Cokugras Haluk Cez |
Case Report: Novel Biallelic Mutations in ARMC4 Cause Primary Ciliary Dyskinesia and Male Infertility in a Chinese Family. Frontiers in genetics 2021 8 12 715339. Gao Yang, Xu Chuan, Tan Qing, Shen Qunshan, Wu Huan, Lv Mingrong, Li Kuokuo, Tang Dongdong, Song Bing, Xu Yuping, Zhou Ping, Wei Zhaolian, Tao Fangbiao, Cao Yunxia, He Xiaoj |
Genetic and Clinical Features of Heterotaxy in a Prenatal Cohort. Frontiers in genetics 2022 5 13 818241. Yi Tong, Sun Hairui, Fu Yuwei, Hao Xiaoyan, Sun Lin, Zhang Ye, Han Jiancheng, Gu Xiaoyan, Liu Xiaowei, Guo Yong, Wang Xin, Zhou Xiaoxue, Zhang Siyao, Yang Qi, Fan Jiaqi, He Yih |
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- Page last updated:Apr 22, 2024
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