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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 25565928)

  • 1. Challenges in clinical diagnosis of williams-beuren syndrome in sub-saharan africans: case reports from cameroon.
    Tekendo-Ngongang C; Dahoun S; Nguefack S; Gimelli S; Sloan-Béna F; Wonkam A
    Mol Syndromol; 2014 Dec; 5(6):287-92. PubMed ID: 25565928
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genome wide array-CGH and qPCR analysis for the identification of genome defects in Williams' syndrome patients in Saudi Arabia.
    Hussein IR; Magbooli A; Huwait E; Chaudhary A; Bader R; Gari M; Ashgan F; Alquaiti M; Abuzenadah A; AlQahtani M
    Mol Cytogenet; 2016; 9():65. PubMed ID: 27525043
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rare genomic rearrangement in a boy with Williams-Beuren syndrome associated to XYY syndrome and intriguing behavior.
    Dutra RL; Piazzon FB; Zanardo ÉA; Costa TV; Montenegro MM; Novo-Filho GM; Dias AT; Nascimento AM; Kim CA; Kulikowski LD
    Am J Med Genet A; 2015 Dec; 167A(12):3197-203. PubMed ID: 26420477
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Clinical aspects and genetics of Williams-Beuren syndrome. Clinical and molecular genetic study of 44 patients with suspected Williams-Beuren syndrome].
    von Beust G; Laccone FA; del Pilar Andrino M; Wessel A
    Klin Padiatr; 2000; 212(6):299-307. PubMed ID: 11190824
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Detection of a Williams Beuren syndrome case by MLPA].
    Laurito S; Branham T; Herrero G; Marsa S; Garro F; Roqué M
    Medicina (B Aires); 2013; 73(1):47-50. PubMed ID: 23335707
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A new diagnosis of Williams-Beuren syndrome in a 49-year-old man with severe bullous emphysema.
    Wojcik MH; Carmichael N; Bieber FR; Wiener DC; Madan R; Pober BR; Raby BA
    Am J Med Genet A; 2017 Aug; 173(8):2235-2239. PubMed ID: 28574231
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical application of chromosomal microarray analysis for the diagnosis of Williams-Beuren syndrome in Chinese Han patients.
    Xia Y; Huang S; Wu Y; Yang Y; Chen S; Li P; Zhuang J
    Mol Genet Genomic Med; 2019 Feb; 7(2):e00517. PubMed ID: 30565396
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genotype-phenotype correlation and the size of microdeletion or microduplication of 7q11.23 region in patients with Williams-Beuren syndrome.
    Ghaffari M; Tahmasebi Birgani M; Kariminejad R; Saberi A
    Ann Hum Genet; 2018 Nov; 82(6):469-476. PubMed ID: 30155880
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Differing Microdeletion Sizes and Breakpoints in Chromosome 7q11.23 in Williams-Beuren Syndrome Detected by Chromosomal Microarray Analysis.
    Li L; Huang L; Luo Y; Huang X; Lin S; Fang Q
    Mol Syndromol; 2016 Feb; 6(6):268-75. PubMed ID: 27022327
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A Novel Recurrent Breakpoint Responsible for Rearrangements in the Williams-Beuren Region.
    Plaja A; Castells N; Cueto-González AM; del Campo M; Vendrell T; Lloveras E; Izquierdo L; Borregan M; Rodríguez-Santiago B; Carrió A; Miró R; Tizzano E
    Cytogenet Genome Res; 2015; 146(3):181-6. PubMed ID: 26382598
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A triplication of the Williams-Beuren syndrome region in a patient with mental retardation, a severe expressive language delay, behavioural problems and dysmorphisms.
    Beunders G; van de Kamp JM; Veenhoven RH; van Hagen JM; Nieuwint AW; Sistermans EA
    J Med Genet; 2010 Apr; 47(4):271-5. PubMed ID: 19752158
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Williams-Beuren Syndrome: Experience of 43 Patients and a Report of an Atypical Case from a Tertiary Care Center in India.
    Sharma P; Gupta N; Chowdhury MR; Phadke SR; Sapra S; Halder A; Ghosh M; Kabra M
    Cytogenet Genome Res; 2015; 146(3):187-94. PubMed ID: 26352091
    [TBL] [Abstract][Full Text] [Related]  

  • 13. No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control.
    Frohnauer J; Caliebe A; Gesk S; Partsch CJ; Siebert R; Pankau R; Jenderny J
    Mol Cytogenet; 2010 Nov; 3():21. PubMed ID: 21054846
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Williams-Beuren syndrome in Mexican patients confirmed by FISH and assessed by aCGH.
    Ramírez-Velazco A; Aguayo-Orozco TA; Figuera L; Rivera H; Jave-Suárez L; Aguilar-Lemarroy A; Torres-Reyes LA; Córdova-Fletes C; Barros-Núñez P; Delgadillo-Pérez S; Dávalos-Rodríguez IP; García-Ortiz JE; Domínguez MG
    J Genet; 2019 Jun; 98(2):. PubMed ID: 31204697
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Development of a Low Cost Semiquantitative Polymerase Chain Reaction Assay for Molecular Diagnosis of Williams Syndrome.
    Ranaweera DM; Silva DC; Samarasinghe D; Perera S; Kugalingam N; Samarasinghe SR; Madushani WY; Jayaweera HHE; Gunewardene S; Muneeswaran K; Gnanam VS; Chandrasekharan NV
    Clin Lab; 2024 Mar; 70(3):. PubMed ID: 38469782
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial Williams-Beuren syndrome ascertained by screening rather than targeted diagnosis.
    Rafati M; Seyyedaboutorabi E; Brujerdi R; Moossavi S; Ghaffari SR
    Clin Dysmorphol; 2012 Jul; 21(3):118-123. PubMed ID: 22473150
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.