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11. Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia. Liu R; Vandiver AR; Harter N; Hogeling M Dermatol Online J; 2021 May; 27(5):. PubMed ID: 34118813 [TBL] [Abstract][Full Text] [Related]
12. Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency. Bergendal B; Norderyd J; Zhou X; Klar J; Dahl N BMC Med Genet; 2016 Nov; 17(1):88. PubMed ID: 27881089 [TBL] [Abstract][Full Text] [Related]
13. Short anagen hair syndrome is caused by mutations in the WNT10A gene and has a genetic overlap with male pattern hair loss. Br J Dermatol; 2023 Nov; 189(6):e112. PubMed ID: 37972136 [No Abstract] [Full Text] [Related]
14. Deleterious Variants in Parveen A; Khan SA; Mirza MU; Bashir H; Arshad F; Iqbal M; Ahmad W; Wahab A; Fiaz A; Naz S; Ashraf F; Mobeen T; Aziz S; Ahmed SS; Muhammad N; Hassib NF; Mostafa MI; Gaboon NE; Gul R; Khan S; Froeyen M; Shoaib M; Wasif N Int J Mol Sci; 2019 Oct; 20(21):. PubMed ID: 31652981 [TBL] [Abstract][Full Text] [Related]
15. WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population. Grejtakova D; Gabrikova-Dojcakova D; Boronova I; Kyjovska L; Hubcejova J; Fecenkova M; Zigova M; Priganc M; Bernasovska J J Genet; 2018 Dec; 97(5):1169-1177. PubMed ID: 30555066 [TBL] [Abstract][Full Text] [Related]
16. WNT10A variants are associated with non-syndromic tooth agenesis in the general population. Song S; Zhao R; He H; Zhang J; Feng H; Lin L Hum Genet; 2014 Jan; 133(1):117-24. PubMed ID: 24043634 [TBL] [Abstract][Full Text] [Related]
17. WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes. Bohring A; Stamm T; Spaich C; Haase C; Spree K; Hehr U; Hoffmann M; Ledig S; Sel S; Wieacker P; Röpke A Am J Hum Genet; 2009 Jul; 85(1):97-105. PubMed ID: 19559398 [TBL] [Abstract][Full Text] [Related]
18. Distinct impacts of bi-allelic WNT10A mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasia. Yu M; Liu Y; Liu H; Wong SW; He H; Zhang X; Wang Y; Han D; Feng H Am J Med Genet A; 2019 Jan; 179(1):57-64. PubMed ID: 30569517 [TBL] [Abstract][Full Text] [Related]
19. WNT10A gene variants at the root of short anagen hair syndrome. Onoufriadis A Br J Dermatol; 2023 Nov; 189(6):653-654. PubMed ID: 37768102 [No Abstract] [Full Text] [Related]
20. Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases. Cluzeau C; Hadj-Rabia S; Jambou M; Mansour S; Guigue P; Masmoudi S; Bal E; Chassaing N; Vincent MC; Viot G; Clauss F; Manière MC; Toupenay S; Le Merrer M; Lyonnet S; Cormier-Daire V; Amiel J; Faivre L; de Prost Y; Munnich A; Bonnefont JP; Bodemer C; Smahi A Hum Mutat; 2011 Jan; 32(1):70-2. PubMed ID: 20979233 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]