91 related articles for article (PubMed ID: 27771473)
1. Williams syndrome and mature B-Leukemia: A random association?
Decimi V; Fazio G; Dell'Acqua F; Maitz S; Galbiati M; Rizzari C; Biondi A; Cazzaniga G; Selicorni A
Eur J Med Genet; 2016 Dec; 59(12):634-640. PubMed ID: 27771473
[TBL] [Abstract][Full Text] [Related]
2. Williams-Beuren Syndrome and Burkitt Leukemia.
Zhukova N; Naqvi A
J Pediatr Hematol Oncol; 2013 Jan; 35(1):e30-2. PubMed ID: 23018576
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Burkitt lymphoma and Ewing sarcoma in a child with Williams syndrome.
Vanhapiha N; Knuutila S; Vettenranta K; Lohi O
Pediatr Blood Cancer; 2014 Oct; 61(10):1877-9. PubMed ID: 24753445
[TBL] [Abstract][Full Text] [Related]
5. Williams-Beuren syndrome in pediatric T-cell acute lymphoblastic leukemia: A rare case report and review of literature.
Yang R; Ai Y; Bai T; Lu XX; He G
Medicine (Baltimore); 2024 Feb; 103(7):e36976. PubMed ID: 38363891
[TBL] [Abstract][Full Text] [Related]
6. Burkitt lymphoma and Williams syndrome: a model for children with a multisystem disorder and malignancy.
Thornburg CD; Roulston D; Castle VP
J Pediatr Hematol Oncol; 2005 Feb; 27(2):109-11. PubMed ID: 15701989
[TBL] [Abstract][Full Text] [Related]
7. Constitutional and somatic deletions of the Williams-Beuren syndrome critical region in non-Hodgkin lymphoma.
Guenat D; Quentin S; Rizzari C; Lundin C; Coliva T; Edery P; Fryssira H; Bermont L; Ferrand C; Soulier J; Borg C; Rohrlich PS
J Hematol Oncol; 2014 Nov; 7():82. PubMed ID: 25388916
[TBL] [Abstract][Full Text] [Related]
8. Single signal of the Williams syndrome chromosome region 1 gene in hyperploidic bone marrow cells of acute lymphoblastic leukemia in a Williams syndrome patient.
Culic V; Culic S; Armanda V; Resic B; Lasan R; Peterlin B
Med Pediatr Oncol; 2002 Mar; 38(3):205-7. PubMed ID: 11836725
[No Abstract] [Full Text] [Related]
9. Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).
Valero MC; de Luis O; Cruces J; Pérez Jurado LA
Genomics; 2000 Oct; 69(1):1-13. PubMed ID: 11013070
[TBL] [Abstract][Full Text] [Related]
10. Williams-Beuren syndrome with brain malformation and hypertrophic cardiomyopathy.
Okamoto N; Yamagata T; Yada Y; Ichihashi K; Matsumoto N; Momoi MY; Mizuguchi T
Brain Dev; 2014 Jun; 36(6):523-7. PubMed ID: 23899771
[TBL] [Abstract][Full Text] [Related]
11. WBSCR14, a putative transcription factor gene deleted in Williams-Beuren syndrome: complete characterisation of the human gene and the mouse ortholog.
de Luis O; Valero MC; Jurado LA
Eur J Hum Genet; 2000 Mar; 8(3):215-22. PubMed ID: 10780788
[TBL] [Abstract][Full Text] [Related]
12. The BCL7 gene family: deletion of BCL7B in Williams syndrome.
Jadayel DM; Osborne LR; Coignet LJ; Zani VJ; Tsui LC; Scherer SW; Dyer MJ
Gene; 1998 Dec; 224(1-2):35-44. PubMed ID: 9931421
[TBL] [Abstract][Full Text] [Related]
13. Pelvic hypoplastic kidney in a patient with Williams-Beuren syndrome.
Stathaki M; Papadopoulou E; Koukouraki S; Sifakis S; Papadaki E; Kalmanti M; Karkavitsas N
Hell J Nucl Med; 2011; 14(2):160-2. PubMed ID: 21761019
[TBL] [Abstract][Full Text] [Related]
14. Autism and Williams syndrome: a case report.
Herguner S; Mukaddes NM
World J Biol Psychiatry; 2006; 7(3):186-8. PubMed ID: 16861145
[TBL] [Abstract][Full Text] [Related]
15. Observation of a parental inversion variant in a rare Williams-Beuren syndrome family with two affected children.
Scherer SW; Gripp KW; Lucena J; Nicholson L; Bonnefont JP; Pérez-Jurado LA; Osborne LR
Hum Genet; 2005 Aug; 117(4):383-8. PubMed ID: 15933846
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes.
Botta A; Novelli G; Mari A; Novelli A; Sabani M; Korenberg J; Osborne LR; Digilio MC; Giannotti A; Dallapiccola B
J Med Genet; 1999 Jun; 36(6):478-80. PubMed ID: 10874638
[TBL] [Abstract][Full Text] [Related]
18. [Extended aortoplasty for supravalvular aortic stenosis with Williams syndrome].
Nagasaka S; Taniguchi S; Kawata T; Mizuguchi K; Kawachi K; Kitamura S
Nihon Kyobu Geka Gakkai Zasshi; 1997 Apr; 45(4):601-6. PubMed ID: 9155132
[TBL] [Abstract][Full Text] [Related]
19. Description of common musculoskeletal findings in Williams Syndrome and implications for therapies.
Copes LE; Pober BR; Terilli CA
Clin Anat; 2016 Jul; 29(5):578-89. PubMed ID: 26749433
[TBL] [Abstract][Full Text] [Related]
20. Sizeable acquired subglottic cyst in a baby with Williams-Beuren syndrome: association or coincidence?
Christoforidis A; Tsakalides C; Chatziavramidis A; Karagianni P; Dimitriadou M; Konstantinidis I
Gene; 2013 Oct; 529(1):148-9. PubMed ID: 23954226
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]