BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

447 related articles for article (PubMed ID: 16861145)

  • 21. Genetic aspects of supravalvular aortic stenosis.
    Morris CA
    Curr Opin Cardiol; 1998 May; 13(3):214-9. PubMed ID: 9649945
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Presenting phenotype and clinical evaluation in a cohort of 22 Williams-Beuren syndrome patients.
    Ferrero GB; Biamino E; Sorasio L; Banaudi E; Peruzzi L; Forzano S; di Cantogno LV; Silengo MC
    Eur J Med Genet; 2007; 50(5):327-37. PubMed ID: 17625998
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Non-Hodgkin lymphoma in a child with Williams syndrome.
    Amenta S; Moschovi M; Sofocleous C; Kostaridou S; Mavrou A; Fryssira H
    Cancer Genet Cytogenet; 2004 Oct; 154(1):86-8. PubMed ID: 15381380
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A novel human gene, WSTF, is deleted in Williams syndrome.
    Lu X; Meng X; Morris CA; Keating MT
    Genomics; 1998 Dec; 54(2):241-9. PubMed ID: 9828126
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome.
    Leme DE; Souza DH; Mercado G; Pastene E; Dias A; Moretti-Ferreira D
    Genet Mol Res; 2013 Sep; 12(3):3407-11. PubMed ID: 24065682
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin.
    Wu YQ; Sutton VR; Nickerson E; Lupski JR; Potocki L; Korenberg JR; Greenberg F; Tassabehji M; Shaffer LG
    Am J Med Genet; 1998 Jun; 78(1):82-9. PubMed ID: 9637430
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Duplication of the Williams-Beuren critical region: case report and further delineation of the phenotypic spectrum.
    Orellana C; Bernabeu J; Monfort S; Roselló M; Oltra S; Ferrer I; Quiroga R; Martínez-Garay I; Martínez F
    J Med Genet; 2008 Mar; 45(3):187-9. PubMed ID: 18310268
    [No Abstract]   [Full Text] [Related]  

  • 29. Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.
    Lukusa T; Vermeesch JR; Holvoet M; Fryns JP; Devriendt K
    Genet Couns; 2004; 15(3):293-301. PubMed ID: 15517821
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Infantile spasms in two children with Williams syndrome.
    Tsao CY; Westman JA
    Am J Med Genet; 1997 Jul; 71(1):54-6. PubMed ID: 9215769
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Williams syndrome--developmental syndrome's common cardiovascular disorders].
    Peippo M; Hiippala A; Raatikka M; Westerlund A; Johansson R; Arvio M; Eronen M
    Duodecim; 2001; 117(5):505-12. PubMed ID: 12116777
    [No Abstract]   [Full Text] [Related]  

  • 32. Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH.
    Goizet C; Excoffier E; Taine L; Taupiac E; El Moneim AA; Arveiler B; Bouvard M; Lacombe D
    Am J Med Genet; 2000 Dec; 96(6):839-44. PubMed ID: 11121193
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Asperger's disorder and Williams syndrome: a case report.
    Kilinçaslan A; Tanidir C; Tutkunkardaş MD; Mukaddes NM
    Turk J Pediatr; 2011; 53(3):352-5. PubMed ID: 21980823
    [TBL] [Abstract][Full Text] [Related]  

  • 34. FISH analysis in both classical and atypical cases of Williams-Beuren syndrome.
    Hou JW; Wang JK; Wang TR
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1998; 39(6):398-403. PubMed ID: 9926515
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Williams-Beuren syndrome: phenotypic variability and deletions of chromosomes 7, 11, and 22 in a series of 52 patients.
    Joyce CA; Zorich B; Pike SJ; Barber JC; Dennis NR
    J Med Genet; 1996 Dec; 33(12):986-92. PubMed ID: 9004128
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Williams-Beuren syndrome: determination of deletion size using quantitative real-time PCR.
    Schubert C; Laccone F
    Int J Mol Med; 2006 Nov; 18(5):799-806. PubMed ID: 17016608
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Williams-Beuren syndrome: unraveling the mysteries of a microdeletion disorder.
    Osborne LR
    Mol Genet Metab; 1999 May; 67(1):1-10. PubMed ID: 10329018
    [No Abstract]   [Full Text] [Related]  

  • 38. Localization of the human HIP1 gene close to the elastin (ELN) locus on 7q11.23.
    Wedemeyer N; Peoples R; Himmelbauer H; Lehrach H; Francke U; Wanker EE
    Genomics; 1997 Dec; 46(2):313-5. PubMed ID: 9417924
    [No Abstract]   [Full Text] [Related]  

  • 39. 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]  

  • 40. Clinical and molecular cytogenetic (FISH) diagnosis of Williams syndrome.
    Brewer CM; Morrison N; Tolmie JL
    Arch Dis Child; 1996 Jan; 74(1):59-61. PubMed ID: 8660051
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 23.