218 related articles for article (PubMed ID: 24398796)
1. Variability in dentofacial phenotypes in four families with WNT10A mutations.
Vink CP; Ockeloen CW; ten Kate S; Koolen DA; Ploos van Amstel JK; Kuijpers-Jagtman AM; van Heumen CC; Kleefstra T; Carels CE
Eur J Hum Genet; 2014 Sep; 22(9):1063-70. PubMed ID: 24398796
[TBL] [Abstract][Full Text] [Related]
2. Case report of Schöpf-Schulz-Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in WNT10A.
Hsu TC; Lee JY; Hsu MM; Chao SC
J Dermatol; 2018 Apr; 45(4):475-478. PubMed ID: 29271000
[TBL] [Abstract][Full Text] [Related]
3. Schöpf-Schulz-Passarge Syndrome: Previously Unreported WNT10A Genotype and Phenotypes in 9 Family Members.
Zimmermann CE; Soufi M; Ruppert V; Schaefer JR; von Domarus H
Acta Derm Venereol; 2019 Jan; 99(1):113-114. PubMed ID: 30265373
[No Abstract] [Full Text] [Related]
4. Schöpf-Schulz-Passarge syndrome associated with two new missense mutations in WNT10A.
Pauly KJ; Balakirski G; Megahed M; Rübben A; Schmitt L
J Dtsch Dermatol Ges; 2018 Jan; 16(1):66-69. PubMed ID: 29314690
[No Abstract] [Full Text] [Related]
5. Schopf-Schulz-Passarge syndrome: a rare ectodermal dysplasia with a delayed diagnosis.
Ismail FF; McGrath J; Sinclair R
Int J Dermatol; 2020 Feb; 59(2):257-258. PubMed ID: 31468502
[No Abstract] [Full Text] [Related]
6. Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.
Tziotzios C; Petrof G; Liu L; Verma A; Wedgeworth EK; Mellerio JE; McGrath JA
Br J Dermatol; 2014 Nov; 171(5):1211-4. PubMed ID: 24902757
[TBL] [Abstract][Full Text] [Related]
7. Eccrine syringofibroadenoma as a clue for the diagnosis of Schöpf-Schulz-Passarge syndrome in acquired palmoplantar keratoderma.
Riera-Monroig J; Martínez-Romero MDC; Alós L; Guillén-Navarro E; Mascaró JM
J Cutan Pathol; 2020 Oct; 47(10):987-989. PubMed ID: 32406069
[No Abstract] [Full Text] [Related]
8. A case of Schöpf-Schulz-Passarge syndrome caused by c.1135C>T WNT10A missense mutation.
Painsi C; Aubell K; Wolf P; Hügel R; Lange-Asschenfeldt B
J Dtsch Dermatol Ges; 2017 Apr; 15(4):455-457. PubMed ID: 28198588
[No Abstract] [Full Text] [Related]
9. Odonto-onycho-dermal dysplasia in a patient homozygous for a WNT10A nonsense mutation and mild manifestations of ectodermal dysplasia in carriers of the mutation.
Krøigård AB; Clemmensen O; Gjørup H; Hertz JM; Bygum A
BMC Dermatol; 2016 Mar; 16():3. PubMed ID: 26964878
[TBL] [Abstract][Full Text] [Related]
10. Genetic study in a suspected case of Schöpf-Schulz-Passarge syndrome.
Vilas-Sueiro A; Monteagudo B; González-Vilas D; Varela-Veiga A; De las Heras C
Indian J Dermatol Venereol Leprol; 2015; 81(4):408-10. PubMed ID: 26087098
[No Abstract] [Full Text] [Related]
11. Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations.
Kantaputra P; Kaewgahya M; Jotikasthira D; Kantaputra W
Am J Med Genet A; 2014 Apr; 164A(4):1041-8. PubMed ID: 24458874
[TBL] [Abstract][Full Text] [Related]
12. Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A.
Petrof G; Fong K; Lai-Cheong JE; Cockayne SE; McGrath JA
Australas J Dermatol; 2011 Aug; 52(3):224-6. PubMed ID: 21834823
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Late diagnosis of ectodermal dysplasia syndrome.
Granger RH; Marshman G; Liu L; McGrath JA
Australas J Dermatol; 2013 Feb; 54(1):46-8. PubMed ID: 22670871
[TBL] [Abstract][Full Text] [Related]
16. Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population.
He H; Han D; Feng H; Qu H; Song S; Bai B; Zhang Z
PLoS One; 2013; 8(11):e80393. PubMed ID: 24312213
[TBL] [Abstract][Full Text] [Related]
17. The WNT10A gene in ectodermal dysplasias and selective tooth agenesis.
Mues G; Bonds J; Xiang L; Vieira AR; Seymen F; Klein O; D'Souza RN
Am J Med Genet A; 2014 Oct; 164A(10):2455-60. PubMed ID: 24700731
[TBL] [Abstract][Full Text] [Related]
18. WNT10A and isolated hypodontia.
Kantaputra P; Sripathomsawat W
Am J Med Genet A; 2011 May; 155A(5):1119-22. PubMed ID: 21484994
[TBL] [Abstract][Full Text] [Related]
19. Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype study.
Tardieu C; Jung S; Niederreither K; Prasad M; Hadj-Rabia S; Philip N; Mallet A; Consolino E; Sfeir E; Noueiri B; Chassaing N; Dollfus H; Manière MC; Bloch-Zupan A; Clauss F
Clin Genet; 2017 Nov; 92(5):477-486. PubMed ID: 28105635
[TBL] [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]