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 *

146 related articles for article (PubMed ID: 34540437)

  • 1. Williams Syndrome With Rare Ureteric Abnormality.
    Khan J; Al-Obaidy KI; Fan R
    Cureus; 2021 Aug; 13(8):e17210. PubMed ID: 34540437
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Variability of the cranial and dental phenotype in Williams syndrome.
    Axelsson S
    Swed Dent J Suppl; 2005; (170):3-67. PubMed ID: 15762376
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Echocardiographic findings in patients with Williams-Beuren syndrome.
    Scheiber D; Fekete G; Urban Z; Tarjan I; Balaton G; Kosa L; Nagy K; Vajo Z
    Wien Klin Wochenschr; 2006 Sep; 118(17-18):538-42. PubMed ID: 17009066
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Congenital heart defects in Williams syndrome.
    Yuan SM
    Turk J Pediatr; 2017; 59(3):225-232. PubMed ID: 29376566
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and genetic characteristics of two cases with Williams-Beuren syndrome.
    Wang LX; Leng J; Li ZH; Yan L; Gou P; Tang F; Su N; Gong CZ; Cheng XR
    Transl Pediatr; 2021 Jun; 10(6):1743-1747. PubMed ID: 34295790
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. [William's syndrome. Report of a case with family involvement].
    Onís Vilches MC; Rubio Cuadrado MV; Martínez de la Iglesia J; López Granados A
    Rev Clin Esp; 1998 Feb; 198(2):91-4. PubMed ID: 9558923
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Surgical Treatment of Adult Williams-Beuren Syndrome with Pulmonary Arteriovenous Fistula.
    Zhang X; Wang S; Huang G
    Heart Surg Forum; 2022 May; 25(3):E381-E384. PubMed ID: 35787765
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cardiovascular spectrum in Williams-Beuren syndrome: the Mexican experience in 40 patients.
    De Rubens Figueroa J; Rodríguez LM; Hach JL; Del Castillo Ruíz V; Martínez HO
    Tex Heart Inst J; 2008; 35(3):279-85. PubMed ID: 18941598
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Diffuse hypoplasia of the aortic arch and isthmus in a patient with Williams syndrome.
    Onan İS; Öztürk E; Demirel Başgöze A; Çicek A; Onan B
    Turk Kardiyol Dern Ars; 2017 Dec; 45(8):758-762. PubMed ID: 29226900
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An unusual combination of an atypical maternally inherited novel 0.3 Mb deletion in Williams-Beuren region and a de novo 22q11.21 microduplication in an infant with supravalvular aortic stenosis.
    Evangelidou P; Kousoulidou L; Salameh N; Alexandrou A; Papaevripidou I; Alexandrou IM; Ketoni A; Ioannidou C; Christophidou-Anastasiadou V; Tanteles GA; Sismani C
    Eur J Med Genet; 2020 Dec; 63(12):104084. PubMed ID: 33045407
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Molecular cytogenetic diagnosis of Williams syndrome.
    Hirota H; Matsuoka R; Kimura M; Imamura S; Joh-o K; Ando M; Takao A; Momma K
    Am J Med Genet; 1996 Aug; 64(3):473-7. PubMed ID: 8862624
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Williams-Beuren syndrome: cardiovascular abnormalities in 20 patients diagnosed with fluorescence in situ hybridization.
    Sugayama SM; Moisés RL; Wagënfur J; Ikari NM; Abe KT; Leone C; da Silva CA; Lopes Ferrari Chauffaille Mde L; Kim CA
    Arq Bras Cardiol; 2003 Nov; 81(5):462-73. PubMed ID: 14666267
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Case of William's Syndrome in a Ugandan Child: A Feasible Diagnosis Even in a Low-Resource Setting.
    Mapelli M; Zagni P; Calbi V; Twalib A; Ferrara R; Agostoni P
    Children (Basel); 2021 Dec; 8(12):. PubMed ID: 34943388
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitral regurgitation without supravalvular aortic stenosis in Williams syndrome.
    Takagi H; Mori Y; Iwata H; Umeda Y; Fukumoto Y; Matsuno Y; Matsutomo M; Shimokawa K; Nishigaki K; Fujiwara H; Hirose H
    Heart Vessels; 2002 Sep; 16(6):257-9. PubMed ID: 12382035
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Computerized Tomography Use in Williams-Beuren Syndrome Aortopathy.
    Kalis NN; Sulaibikh LK; Al Amer SR; Al Amer HY
    Heart Views; 2017; 18(1):21-25. PubMed ID: 28584589
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Atypical Williams syndrome in an infant with complete atrioventricular canal defect.
    Ahrens-Nicklas RC; Reichert SL; Zackai EH; Kaplan PB
    Am J Med Genet A; 2015 Dec; 167A(12):3108-12. PubMed ID: 26271350
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Long-term cardiovascular outcome of Williams syndrome.
    Cha SG; Song MK; Lee SY; Kim GB; Kwak JG; Kim WH; Bae EJ
    Congenit Heart Dis; 2019 Sep; 14(5):684-690. PubMed ID: 31166070
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.