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.
191 related articles for article (PubMed ID: 9345098)
1. Mutation characterization and genotype-phenotype correlation in Barth syndrome. Johnston J; Kelley RI; Feigenbaum A; Cox GF; Iyer GS; Funanage VL; Proujansky R Am J Hum Genet; 1997 Nov; 61(5):1053-8. PubMed ID: 9345098 [TBL] [Abstract][Full Text] [Related]
2. Novel missense mutation (R94S) in the TAZ ( G4.5) gene in a Japanese patient with Barth syndrome. Sakamoto O; Kitoh T; Ohura T; Ohya N; Iinuma K J Hum Genet; 2002; 47(5):229-31. PubMed ID: 12032589 [TBL] [Abstract][Full Text] [Related]
3. Genetic analysis of the G4.5 gene in families with suspected Barth syndrome. Cantlay AM; Shokrollahi K; Allen JT; Lunt PW; Newbury-Ecob RA; Steward CG J Pediatr; 1999 Sep; 135(3):311-5. PubMed ID: 10484795 [TBL] [Abstract][Full Text] [Related]
4. Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction. Chen R; Tsuji T; Ichida F; Bowles KR; Yu X; Watanabe S; Hirono K; Tsubata S; Hamamichi Y; Ohta J; Imai Y; Bowles NE; Miyawaki T; Towbin JA; Mol Genet Metab; 2002 Dec; 77(4):319-25. PubMed ID: 12468278 [TBL] [Abstract][Full Text] [Related]
5. A novel mutation in the G4.5 (TAZ) gene in a Greek patient with Barth syndrome. Bachou T; Giannakopoulos A; Trapali C; Vazeou A; Kattamis A Blood Cells Mol Dis; 2009; 42(3):262-4. PubMed ID: 19261493 [TBL] [Abstract][Full Text] [Related]
6. New clinical and molecular insights on Barth syndrome. Ferri L; Donati MA; Funghini S; Malvagia S; Catarzi S; Lugli L; Ragni L; Bertini E; Vaz FM; Cooper DN; Guerrini R; Morrone A Orphanet J Rare Dis; 2013 Feb; 8():27. PubMed ID: 23409742 [TBL] [Abstract][Full Text] [Related]
7. A novel mutation in the G4.5 (TAZ) gene in a kindred with Barth syndrome. Vesel S; Stopar-Obreza M; Trebusak-Podkrajsek K; Jazbec J; Podnar T; Battelino T Eur J Hum Genet; 2003 Jan; 11(1):97-101. PubMed ID: 12529714 [TBL] [Abstract][Full Text] [Related]
8. Barth syndrome: TAZ gene mutations, mRNAs, and evolution. Gonzalez IL Am J Med Genet A; 2005 May; 134(4):409-14. PubMed ID: 15793838 [TBL] [Abstract][Full Text] [Related]
9. Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome. Ichida F; Tsubata S; Bowles KR; Haneda N; Uese K; Miyawaki T; Dreyer WJ; Messina J; Li H; Bowles NE; Towbin JA Circulation; 2001 Mar; 103(9):1256-63. PubMed ID: 11238270 [TBL] [Abstract][Full Text] [Related]
10. A novel X-linked gene, G4.5. is responsible for Barth syndrome. Bione S; D'Adamo P; Maestrini E; Gedeon AK; Bolhuis PA; Toniolo D Nat Genet; 1996 Apr; 12(4):385-9. PubMed ID: 8630491 [TBL] [Abstract][Full Text] [Related]
11. X chromosome inactivation in carriers of Barth syndrome. Orstavik KH; Orstavik RE; Naumova AK; D'Adamo P; Gedeon A; Bolhuis PA; Barth PG; Toniolo D Am J Hum Genet; 1998 Nov; 63(5):1457-63. PubMed ID: 9792874 [TBL] [Abstract][Full Text] [Related]
12. Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28. Adès LC; Gedeon AK; Wilson MJ; Latham M; Partington MW; Mulley JC; Nelson J; Lui K; Sillence DO Am J Med Genet; 1993 Feb; 45(3):327-34. PubMed ID: 8434619 [TBL] [Abstract][Full Text] [Related]
13. The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies. D'Adamo P; Fassone L; Gedeon A; Janssen EA; Bione S; Bolhuis PA; Barth PG; Wilson M; Haan E; Orstavik KH; Patton MA; Green AJ; Zammarchi E; Donati MA; Toniolo D Am J Hum Genet; 1997 Oct; 61(4):862-7. PubMed ID: 9382096 [TBL] [Abstract][Full Text] [Related]
18. X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome. Gedeon AK; Wilson MJ; Colley AC; Sillence DO; Mulley JC J Med Genet; 1995 May; 32(5):383-8. PubMed ID: 7616547 [TBL] [Abstract][Full Text] [Related]
19. A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth Syndrome. Fan Y; Steller J; Gonzalez IL; Kulik W; Fox M; Chang R; Westerfield BA; Batra AS; Wang RY; Gallant NM; Pena LS; Wang H; Huang T; Bhuta S; Penny DJ; McCabe ER; Kimonis VE JIMD Rep; 2013; 11():99-106. PubMed ID: 23606313 [TBL] [Abstract][Full Text] [Related]
20. Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28. Bolhuis PA; Hensels GW; Hulsebos TJ; Baas F; Barth PG Am J Hum Genet; 1991 Mar; 48(3):481-5. PubMed ID: 1998334 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]