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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 - 3 (of 3 Records)

Query Trace: Disease and NTN1[original query]
DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.
Human molecular genetics 2017 12 27 (2): 359-372.
Bouilly Justine, Messina Andrea, Papadakis Georgios, Cassatella Daniele, Xu Cheng, Acierno James S, Tata Brooke, Sykiotis Gerasimos, Santini Sara, Sidis Yisrael, Elowe-Gruau Eglantine, Phan-Hug Franziska, Hauschild Michael, Bouloux Pierre-Marc, Quinton Richard, Lang-Muritano Mariarosaria, Favre Lucie, Marino Laura, Giacobini Paolo, Dwyer Andrew A, Niederländer Nicolas J, Pitteloud Nel
Association of genetic polymorphisms of VAX1, MAFB, and NTN1 with nonsyndromic cleft lip with or without cleft palate in Chinese population.
Molecular genetics and genomics : MGG 2022 Feb .
Peng Li, Niu Zhenmin, Chen Jiapei, Wan Teng, Wu Dandan, Yang Yusheng, Wang Guomin, Yang Lin, Huang Wei, Chen Zhen
Identification of putative regulatory single-nucleotide variants in NTN1 gene associated with NSCL/P.
Journal of human genetics 2023 3 .
Tao Hong-Xu, Yang Yi-Xin, Shi Bing, Jia Zhong-L
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