130 related articles for article (PubMed ID: 37869104)
1. Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation.
Murshidi R; Al-Lala H
Case Rep Dermatol Med; 2023; 2023():5577379. PubMed ID: 37869104
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Mutation-Proved Clouston Syndrome in a Large Indian Family with a Variant Phenotype.
Khatter S; Puri RD; Mahay SB; Bhai P; Saxena R; Verma IC
Indian J Dermatol; 2019; 64(2):143-145. PubMed ID: 30983611
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Clouston syndrome: first case in Russia.
Marakhonov A; Skoblov M; Galkina V; Zinchenko R
Balkan J Med Genet; 2012 Jun; 15(1):51-4. PubMed ID: 24052723
[TBL] [Abstract][Full Text] [Related]
7. GJB6, of which mutations underlie Clouston syndrome, is a potential direct target gene of p63.
Fujimoto A; Kurban M; Nakamura M; Farooq M; Fujikawa H; Kibbi AG; Ito M; Dahdah M; Matta M; Diab H; Shimomura Y
J Dermatol Sci; 2013 Feb; 69(2):159-66. PubMed ID: 23219093
[TBL] [Abstract][Full Text] [Related]
8. Do you know this syndrome? Clouston syndrome.
Sanches S; Rebellato PRO; Fabre AB; Campos GLM
An Bras Dermatol; 2017; 92(3):417-418. PubMed ID: 29186264
[TBL] [Abstract][Full Text] [Related]
9. Phenotypic variability in gap junction syndromic skin disorders: experience from KID and Clouston syndromes' clinical diagnostics.
Kutkowska-Kaźmierczak A; Niepokój K; Wertheim-Tysarowska K; Giza A; Mordasewicz-Goliszewska M; Bal J; Obersztyn E
J Appl Genet; 2015 Aug; 56(3):329-37. PubMed ID: 25575739
[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. Genetic heterogeneity of KID syndrome: identification of a Cx30 gene (GJB6) mutation in a patient with KID syndrome and congenital atrichia.
Jan AY; Amin S; Ratajczak P; Richard G; Sybert VP
J Invest Dermatol; 2004 May; 122(5):1108-13. PubMed ID: 15140211
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. A patient with alopecia, nail dystrophy, palmoplantar hyperkeratosis, keratitis, hearing difficulty and micrognathia without GJB2 or GJB6 mutations: a new type of hidrotic ectodermal dysplasia?
Nakamura M; Ishikawa O
Br J Dermatol; 2007 Apr; 156(4):777-9. PubMed ID: 17298485
[No Abstract] [Full Text] [Related]
15. The Clinical Manifestation of p.Asp50Asn Heterozygous Mutation of
Xu Y; Wang M; Huang L; Hu J
Ann Dermatol; 2022 Oct; 34(5):382-386. PubMed ID: 36198631
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A novel variant in the GJB6 gene in a large Chinese family with a unique phenotype of Clouston syndrome.
Huang H; Chen M; Liu X; Xiong X; Zhou L; Su Z; Lu Y; Liang B
Front Med; 2023 Apr; 17(2):330-338. PubMed ID: 36645631
[TBL] [Abstract][Full Text] [Related]
18. Clouston syndrome: a rare autosomal dominant trait with palmoplantar hyperkeratosis and alopecia.
Patel RR; Bixler D; Norins AL
J Craniofac Genet Dev Biol; 1991; 11(3):176-9. PubMed ID: 1837030
[TBL] [Abstract][Full Text] [Related]
19. 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]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
