These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 24398796)

  • 21. Schöpf-Schulz-Passarge syndrome with an unusual pattern of inheritance.
    Craigen WJ; Levy ML; Lewis RA
    Am J Med Genet; 1997 Aug; 71(2):186-8. PubMed ID: 9217219
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Long-term dental management of a patient with features of Schöpf-Schulz-Passarge syndrome.
    Manchanda N; Anthonappa R; Al-Mulla H; King N
    Spec Care Dentist; 2017 Jul; 37(4):204-208. PubMed ID: 28598512
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Early diagnosis of Schöpf-Schulz-Passarge syndrome by whole-exome sequencing: the first Chinese case.
    Ren JN; Su H; Xue RZ; Chen YF
    J Eur Acad Dermatol Venereol; 2022 Sep; 36(9):e722-e724. PubMed ID: 35592912
    [No Abstract]   [Full Text] [Related]  

  • 24. Schöpf-Schulz-Passarge syndrome: further delineation of the phenotype and genetic considerations.
    Castori M; Ruggieri S; Giannetti L; Annessi G; Zambruno G
    Acta Derm Venereol; 2008; 88(6):607-12. PubMed ID: 19002348
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum.
    Castori M; Castiglia D; Brancati F; Foglio M; Heath S; Floriddia G; Madonna S; Fischer J; Zambruno G
    Clin Genet; 2011 Jan; 79(1):92-5. PubMed ID: 21143469
    [No Abstract]   [Full Text] [Related]  

  • 26. Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A.
    Nagy N; Wedgeworth E; Hamada T; White JM; Hashimoto T; McGrath JA
    J Dermatol Sci; 2010 Jun; 58(3):220-2. PubMed ID: 20418069
    [No Abstract]   [Full Text] [Related]  

  • 27. WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome.
    Nawaz S; Klar J; Wajid M; Aslam M; Tariq M; Schuster J; Baig SM; Dahl N
    Eur J Hum Genet; 2009 Dec; 17(12):1600-5. PubMed ID: 19471313
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Multiple eccrine hydrocystomas of the eyelids in the framework of Schöpf syndrome. A case report].
    Dot C; Dordain M; Boucher E; Metge F; Millet P; Maille M; Maurin J
    J Fr Ophtalmol; 2000 Oct; 23(8):809-16. PubMed ID: 11033504
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [WNT 10A-mutations as explanation for tooth agenesis].
    Backaert H; Carels CE
    Ned Tijdschr Tandheelkd; 2014 Nov; 121(11):541-4. PubMed ID: 26188476
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.
    Plaisancié J; Bailleul-Forestier I; Gaston V; Vaysse F; Lacombe D; Holder-Espinasse M; Abramowicz M; Coubes C; Plessis G; Faivre L; Demeer B; Vincent-Delorme C; Dollfus H; Sigaudy S; Guillén-Navarro E; Verloes A; Jonveaux P; Martin-Coignard D; Colin E; Bieth E; Calvas P; Chassaing N
    Am J Med Genet A; 2013 Apr; 161A(4):671-8. PubMed ID: 23401279
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutations in WNT10A are present in more than half of isolated hypodontia cases.
    van den Boogaard MJ; Créton M; Bronkhorst Y; van der Hout A; Hennekam E; Lindhout D; Cune M; Ploos van Amstel HK
    J Med Genet; 2012 May; 49(5):327-31. PubMed ID: 22581971
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia.
    Adaimy L; Chouery E; Megarbane H; Mroueh S; Delague V; Nicolas E; Belguith H; de Mazancourt P; Megarbane A
    Am J Hum Genet; 2007 Oct; 81(4):821-8. PubMed ID: 17847007
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population.
    Martínez-Romero MC; Ballesta-Martínez MJ; López-González V; Sánchez-Soler MJ; Serrano-Antón AT; Barreda-Sánchez M; Rodriguez-Peña L; Martínez-Menchon MT; Frías-Iniesta J; Sánchez-Pedreño P; Carbonell-Meseguer P; Glover-López G; Guillén-Navarro E;
    Orphanet J Rare Dis; 2019 Dec; 14(1):281. PubMed ID: 31796081
    [TBL] [Abstract][Full Text] [Related]  

  • 35. WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity.
    Kantaputra P; Kaewgahya M; Kantaputra W
    Am J Med Genet A; 2014 Feb; 164A(2):360-3. PubMed ID: 24311251
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Schöpf-Schulz-Passarge syndrome with multiple angiomas on the tongue: a new feature?
    Trocoli Drakensjö I; Björck E; Bradley M; Hedblad MA
    Int J Dermatol; 2021 May; 60(5):641-642. PubMed ID: 33355925
    [No Abstract]   [Full Text] [Related]  

  • 37. Novel mutations identified in patients with tooth agenesis by whole-exome sequencing.
    Zhao K; Lian M; Zou D; Huang W; Zhou W; Shen Y; Wang F; Wu Y
    Oral Dis; 2019 Mar; 25(2):523-534. PubMed ID: 30417976
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families.
    Issa YA; Kamal L; Rayyan AA; Dweik D; Pierce S; Lee MK; King MC; Walsh T; Kanaan M
    Eur J Hum Genet; 2016 Oct; 24(10):1430-5. PubMed ID: 27049303
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia.
    Liu Y; Sun J; Zhang C; Wu Y; Ma S; Li X; Wu X; Gao Q
    BMC Oral Health; 2024 Jan; 24(1):136. PubMed ID: 38280992
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.