BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

114 related articles for article (PubMed ID: 10730756)

  • 1. Refined localization of the gene for Clouston syndrome (hidrotic ectodermal dysplasia) in a large French family.
    Lamartine J; Laoudj D; Blanchet-Bardon C; Kibar Z; Soularue P; Ridoux V; Dubertret L; Rouleau GA; Waksman G
    Br J Dermatol; 2000 Feb; 142(2):248-52. PubMed ID: 10730756
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Confirmation of linkage of Clouston syndrome (hidrotic ectodermal dysplasia) to 13q11-q12.1 with evidence for multiple independent mutations.
    Taylor TD; Hayflick SJ; McKinnon W; Guttmacher AE; Hovnanian A; Litt M; Zonana J
    J Invest Dermatol; 1998 Jul; 111(1):83-5. PubMed ID: 9665391
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q.
    Kibar Z; Der Kaloustian VM; Brais B; Hani V; Fraser FC; Rouleau GA
    Hum Mol Genet; 1996 Apr; 5(4):543-7. PubMed ID: 8845850
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region.
    Radhakrishna U; Blouin JL; Mehenni H; Mehta TY; Sheth FJ; Sheth JJ; Solanki JV; Antonarakis SE
    Am J Med Genet; 1997 Jul; 71(1):80-6. PubMed ID: 9215774
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping.
    Kibar Z; Dubé MP; Powell J; McCuaïg C; Hayflick SJ; Zonana J; Hovnanian A; Radhakrishna U; Antonarakis SE; Benohanian A; Sheeran AD; Stephan ML; Gosselin R; Kelsell DP; Christianson AL; Fraser FC; Der Kaloustian VM; Rouleau GA
    Eur J Hum Genet; 2000 May; 8(5):372-80. PubMed ID: 10854098
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clouston syndrome (hidrotic ectodermal dysplasia) is not linked to keratin gene clusters on chromosomes 12 and 17.
    Hayflick SJ; Taylor T; McKinnon W; Guttmacher AE; Litt M; Zonana J
    J Invest Dermatol; 1996 Jul; 107(1):11-4. PubMed ID: 8752831
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A 1.5-Mb physical map of the hidrotic ectodermal dysplasia (Clouston syndrome) gene region on human chromosome 13q11.
    Lamartine J; Pitaval A; Soularue P; Lanneluc I; Lemaître G; Kibar Z; Rouleau GA; Waksman G
    Genomics; 2000 Jul; 67(2):232-6. PubMed ID: 10903849
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A mutation in the connexin 30 gene in Chinese Han patients with hidrotic ectodermal dysplasia.
    Zhang XJ; Chen JJ; Yang S; Cui Y; Xiong XY; He PP; Dong PL; Xu SJ; Li YB; Zhou Q; Wang Y; Huang W
    J Dermatol Sci; 2003 Jun; 32(1):11-7. PubMed ID: 12788524
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A radiation hybrid map of 48 loci including the clouston hidrotic ectodermal dysplasia locus in the pericentromeric region of chromosome 13q.
    Kibar Z; Lafrenière RG; Chakravarti A; Wang JC; Chevrette M; Der Kaloustian VM; Rouleau GA
    Genomics; 1999 Feb; 56(1):127-30. PubMed ID: 10036193
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A recurrent mutation of GJB6 in a big Chinese family with Hidrotic ectodermal dysplasia.
    Zhan Y; Luo S; Pi Z; Zhang G
    Hereditas; 2020 Aug; 157(1):34. PubMed ID: 32843087
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of a known GJB6 mutation in an autosomal dominant inherited Chinese family with hidrotic ectodermal dysplasia.
    Mousumi T; Xiong Z; Lu L; Liu S; Xia K; Hu Z
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2013 Aug; 38(8):761-5. PubMed ID: 23981984
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diffuse Palmoplantar Keratoderma, Onychodystrophy, universal Hypotrichosis and Cysts.
    Arif T; Amin SS; Adil M; Mohtashim M
    Acta Dermatovenerol Croat; 2017 Jul; 25(2):161-163. PubMed ID: 28871934
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel mutations in GJB6 and GJB2 in Clouston syndrome.
    Liu YT; Guo K; Li J; Liu Y; Zeng WH; Geng SM
    Clin Exp Dermatol; 2015 Oct; 40(7):770-3. PubMed ID: 25808784
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel connexin 30 mutation in Clouston syndrome.
    Smith FJ; Morley SM; McLean WH
    J Invest Dermatol; 2002 Mar; 118(3):530-2. PubMed ID: 11874494
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Refined mapping of Naegeli-Franceschetti- Jadassohn syndrome to a 6 cM interval on chromosome 17q11.2-q21 and investigation of candidate genes.
    Sprecher E; Itin P; Whittock NV; McGrath JA; Meyer R; DiGiovanna JJ; Bale SJ; Uitto J; Richard G
    J Invest Dermatol; 2002 Sep; 119(3):692-8. PubMed ID: 12230514
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A known mutation in GJB6 in a large Chinese family with hidrotic ectodermal dysplasia.
    Yang R; Hu Z; Kong Q; Li W; Zhang L; Du X; Huang S; Xia X; Sang H
    J Eur Acad Dermatol Venereol; 2016 Aug; 30(8):1362-5. PubMed ID: 27137747
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1.
    Rafiq MA; Faiyaz-Ul-Haque M; Ud Din MA; Malik S; Sohail M; Anwar M; Haque S; Paterson AD; Tsui LC; Ahmad W
    J Invest Dermatol; 2005 Feb; 124(2):338-42. PubMed ID: 15675952
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel mutations in the EDAR gene in two Pakistani consanguineous families with autosomal recessive hypohidrotic ectodermal dysplasia.
    Naeem M; Muhammad D; Ahmad W
    Br J Dermatol; 2005 Jul; 153(1):46-50. PubMed ID: 16029325
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation.
    Rasool M; Nawaz S; Azhar A; Wajid M; Westermark P; Baig SM; Klar J; Dahl N
    Eur J Dermatol; 2010; 20(4):443-6. PubMed ID: 20409997
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3.
    Tariq M; Chishti MS; Ali G; Ahmad W
    Ann Hum Genet; 2008 Jan; 72(Pt 1):19-25. PubMed ID: 18184143
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.