BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 26429123)

  • 21. Intrauterine phenotype features of fetuses with Williams-Beuren syndrome and literature review.
    Yuan M; Deng L; Yang Y; Sun L
    Ann Hum Genet; 2020 Mar; 84(2):169-176. PubMed ID: 31711272
    [TBL] [Abstract][Full Text] [Related]  

  • 22. FISH analysis in patients with clinical diagnosis of Williams syndrome.
    Elçioglu N; Mackie-Ogilvie C; Daker M; Berry AC
    Acta Paediatr; 1998 Jan; 87(1):48-53. PubMed ID: 9510447
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Clinical and genetic characteristics of Williams-Beuren syndrome: 2 cases report].
    Wang SQ; Yang ZX; Li H
    Beijing Da Xue Xue Bao Yi Xue Ban; 2017 Oct; 49(5):899-903. PubMed ID: 29045977
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Clinical characterization, molecular and FISH studies in 80 patients with clinical suspicion of Williams-Beuren syndrome].
    Milà M; Carrió A; Sánchez A; Gómez D; Jiménez D; Estivill X; Ballesta F
    Med Clin (Barc); 1999 Jun; 113(2):46-9. PubMed ID: 10425618
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Severe left main coronary artery stenosis with abnormal branching pattern in a patient with mild supravalvar aortic stenosis and Williams-Beuren syndrome.
    Pieles GE; Ofoe V; Morgan GJ
    Congenit Heart Dis; 2014; 9(3):E85-9. PubMed ID: 23701710
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Keratoconus associated with Williams-Beuren syndrome: first case reports.
    Pinsard L; Touboul D; Vu Y; Lacombe D; Leger F; Colin J
    Ophthalmic Genet; 2010 Dec; 31(4):252-6. PubMed ID: 21067490
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A case report of rapid progressive coarctation and severe middle aortic syndrome in an infant with Williams syndrome.
    Hall EK; Glatz J; Kaplan P; Kaplan BS; Hellinger J; Ernst L; Gaynor JW
    Congenit Heart Dis; 2009; 4(5):373-7. PubMed ID: 19740193
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Investigation of deletions at 7q11.23 in 44 patients referred for Williams-Beuren syndrome, using FISH and four DNA polymorphisms.
    Brøndum-Nielsen K; Beck B; Gyftodimou J; Hørlyk H; Liljenberg U; Petersen MB; Pedersen W; Petersen MB; Sand A; Skovby F; Stafanger G; Zetterqvist P; Tommerup N
    Hum Genet; 1997 Jan; 99(1):56-61. PubMed ID: 9003495
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Williams-Beuren Syndrome: A Clinical Study of 55 Brazilian Patients and the Diagnostic Use of MLPA.
    Honjo RS; Dutra RL; Furusawa EA; Zanardo EA; Costa LS; Kulikowski LD; Bertola DR; Kim CA
    Biomed Res Int; 2015; 2015():903175. PubMed ID: 26090456
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Elastin mutation screening in a group of patients affected by vascular abnormalities.
    Rodriguez-Revenga L; Badenas C; Carrió A; Milà M
    Pediatr Cardiol; 2005; 26(6):827-31. PubMed ID: 15990952
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Williams-Beuren syndrome in the Hong Kong Chinese population: retrospective study.
    Yau EK; Lo IF; Lam ST
    Hong Kong Med J; 2004 Feb; 10(1):22-7. PubMed ID: 14967851
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Genetic analysis of a child with atypical Williams-Beuren syndrome presenting as supravalvular aortic stenosis].
    Wu D; Zhang M; Gao Y; Huo X; Xiao H; Zhang Q; Kang B; Wang X; Liao S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):475-478. PubMed ID: 32219841
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Severely calcified valvular aortic stenosis firstly diagnosed in monozygotic male twins with suspected Williams-Beuren syndrome.
    Yetkin U; Bal F; Bayata S; Gürbüz A
    Jpn Heart J; 2004 Sep; 45(5):877-83. PubMed ID: 15557730
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Rapid progression of long-segment coarctation in a patient with Williams' syndrome.
    Arrington C; Tristani-Firouzi M; Puchalski M
    Cardiol Young; 2005 Jun; 15(3):312-4. PubMed ID: 15865838
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Molecular and phenotypic characterization of atypical Williams-Beuren syndrome.
    Euteneuer J; Carvalho CM; Kulkarni S; Vineyard M; Grady RM; Lupski JR; Shinawi M
    Clin Genet; 2014 Nov; 86(5):487-91. PubMed ID: 24246242
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the elastin locus.
    Kotzot D; Bernasconi F; Brecevic L; Robinson WP; Kiss P; Kosztolanyi G; Lurie IW; Superti-Furga A; Schinzel A
    Eur J Pediatr; 1995 Jun; 154(6):477-82. PubMed ID: 7545578
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Atypical deletions in Williams-Beuren syndrome].
    Ramírez-Velazco A; Domínguez-Quezada MG
    Rev Med Inst Mex Seguro Soc; 2017; 55(5):615-620. PubMed ID: 29193944
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A new case of keratoconus associated with Williams-Beuren syndrome.
    Viana MM; Frasson M; Leão LL; Stofanko M; Gonçalves-Dornelas H; Cunha Pda S; de Aguiar MJ
    Ophthalmic Genet; 2013 Sep; 34(3):174-7. PubMed ID: 23167938
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Fluorescent in situ hybridisation (FISH) for hemizygous deletion at the elastin locus in patients with isolated supravalvular aortic stenosis.
    Fryssira H; Palmer R; Hallidie-Smith KA; Taylor J; Donnai D; Reardon W
    J Med Genet; 1997 Apr; 34(4):306-8. PubMed ID: 9138154
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Genetic diagnosis of Williams syndrome].
    Urbán Z; Kiss E; Kádár K; Szabolcs J; Csiszár K; Boyd DC; Fekete G
    Orv Hetil; 1997 Jul; 138(27):1749-52. PubMed ID: 9273487
    [TBL] [Abstract][Full Text] [Related]  

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