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Journal Abstract Search

401 related items for PubMed ID: 24312213

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  • 4. 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, GIEDE (Spanish multidisciplinary research group for ectodermal dysplasia).
    Orphanet J Rare Dis; 2019 Dec 03; 14(1):281. PubMed ID: 31796081
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  • 6. Gene Mutations of the Three Ectodysplasin Pathway Key Players (EDA, EDAR, and EDARADD) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations.
    Ahmed HA, El-Kamah GY, Rabie E, Mostafa MI, Abouzaid MR, Hassib NF, Mehrez MI, Abdel-Kader MA, Mohsen YH, Zada SK, Amr KS, Sayed ISM.
    Genes (Basel); 2021 Sep 08; 12(9):. PubMed ID: 34573371
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    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Wright JT, Grange DK, Fete M.
    ; 1993 Sep 08. PubMed ID: 20301291
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  • 9. Missense mutations in EDA and EDAR genes cause dominant syndromic tooth agenesis.
    Andreoni F, Sgattoni C, Bencardino D, Simonetti O, Forabosco A, Magnani M.
    Mol Genet Genomic Med; 2021 Jan 08; 9(1):e1555. PubMed ID: 33205897
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  • 13. Novel EDA or EDAR Mutations Identified in Patients with X-Linked Hypohidrotic Ectodermal Dysplasia or Non-Syndromic Tooth Agenesis.
    Zeng B, Zhao Q, Li S, Lu H, Lu J, Ma L, Zhao W, Yu D.
    Genes (Basel); 2017 Oct 05; 8(10):. PubMed ID: 28981473
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  • 14. From ectodermal dysplasia to selective tooth agenesis.
    Mues GI, Griggs R, Hartung AJ, Whelan G, Best LG, Srivastava AK, D'Souza R.
    Am J Med Genet A; 2009 Sep 05; 149A(9):2037-41. PubMed ID: 19504606
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  • 15. De novo EDA mutations: Variable expression in two Egyptian families.
    Gaczkowska A, Abdalla EM, Dowidar KM, Elhady GM, Jagodzinski PP, Mostowska A.
    Arch Oral Biol; 2016 Aug 05; 68():21-8. PubMed ID: 27054699
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  • 17. Eight EDA mutations in Chinese patients with tooth agenesis and genotype-phenotype analysis.
    Yu K, Sheng Y, Wang F, Yang S, Wan F, Lei M, Wu Y.
    Oral Dis; 2024 Oct 05; 30(7):4598-4607. PubMed ID: 38287639
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  • 18. Whole genome sequencing reveals novel non-synonymous mutation in ectodysplasin A (EDA) associated with non-syndromic X-linked dominant congenital tooth agenesis.
    Sarkar T, Bansal R, Das P.
    PLoS One; 2014 Oct 05; 9(9):e106811. PubMed ID: 25203534
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