Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Ectodermal Dysplasia and WNT10A[original query] |
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| Mutations in WNT10A are present in more than half of isolated hypodontia cases. Journal of medical genetics 2012 May 49 (5): 327-31. van den Boogaard Marie-José, Créton Marijn, Bronkhorst Yvon, van der Hout Annemieke, Hennekam Eric, Lindhout Dick, Cune Marco, Ploos van Amstel Hans Kristi |
| Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia. American journal of medical genetics. Part A 2013 Apr 161A (4): 671-8. Plaisancié Julie, Bailleul-Forestier Isabelle, Gaston Véronique, Vaysse Fréderic, Lacombe Didier, Holder-Espinasse Muriel, Abramowicz Marc, Coubes Christine, Plessis Ghislaine, Faivre Laurence, Demeer Bénédicte, Vincent-Delorme Catherine, Dollfus Hélène, Sigaudy Sabine, Guillén-Navarro Encarna, Verloes Alain, Jonveaux Philippe, Martin-Coignard Dominique, Colin Estelle, Bieth Eric, Calvas Patrick, Chassaing Nicol |
| Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population. PloS one 2013 8 (11): e80393. He Huiying, Han Dong, Feng Hailan, Qu Hong, Song Shujuan, Bai Baojing, Zhang Zhenti |
| Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients. Genes 2016 7 (9): . Zeng Binghui, Xiao Xue, Li Sijie, Lu Hui, Lu Jiaxuan, Zhu Ling, Yu Dongsheng, Zhao W |
| Turkish Ectodermal Dysplasia Cohort: From Phenotype to Genotype in 17 Families. Cytogenetic and genome research 2019 4 157 (4): 189-196. Güven Yeliz, Bal Elodie, Altunoglu Umut, Yücel Esra, Hadj-Rabia Smail, Koruyucu Mine, Bahar Tuna Elif, Ç?ld?r ?ule, Aktören Oya, Bodemer Christine, Uyguner Zehra O, Smahi Asma, Kayserili Hül |
| EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population. Orphanet journal of rare diseases 2019 12 14 (1): 281. Martínez-Romero María Carmen, Ballesta-Martínez María Juliana, López-González Vanesa, Sánchez-Soler María José, Serrano-Antón Ana Teresa, Barreda-Sánchez María, Rodriguez-Peña Lidya, Martínez-Menchon María Teresa, Frías-Iniesta José, Sánchez-Pedreño Paloma, Carbonell-Meseguer Pablo, Glover-López Guillermo, Guillén-Navarro Encarna, |
| Short anagen hair syndrome: Association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss. The British journal of dermatology 2023 9 . Nicole Cesarato, Agnes Schwieger-Briel, Yasmina Gossmann, Sabrina K Henne, Kathrin Hillmann, Leonie H Frommherz, Maria Wehner, Xing Xiong, Holger Thiele, Vinzenz Oji, Donatella Milani, Iliana Tantcheva-Poor, Kathrin Giehl, Regina Fölster-Holst, Anne Teichler, Delphine Braeckmans, Peter H Hoeger, Gabriela Jones, Jorge Frank, Lisa Weibel, Ulrike Blume-Peytavi, Henning Hamm, Markus M Nöthen, Matthias Geyer, Stefanie Heilmann-Heimbach, F Buket Basmanav, Regina C Be |
| Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia. BMC oral health 2024 1 24 (1): 136. Yiting Liu, Jing Sun, Caiqi Zhang, Yi Wu, Siyuan Ma, Xuechun Li, Xiaoshan Wu, Qingping G |
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