Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 126

1.

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. doi: 10.1002/pbc.25055. Epub 2014 Apr 19.

PMID:
24753445
2.

Williams-Beuren Syndrome and Burkitt Leukemia.

Zhukova N, Naqvi A.

J Pediatr Hematol Oncol. 2013 Jan;35(1):e30-2. doi: 10.1097/MPH.0b013e318270672f.

PMID:
23018576
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 1;154(1):86-8.

PMID:
15381380
4.

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.

PMID:
15701989
5.

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;7:82. doi: 10.1186/s13045-014-0082-4.

6.

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. doi: 10.1002/ajmg.a.37360. Epub 2015 Sep 30.

PMID:
26420477
7.

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. doi: 10.1016/j.ejmg.2016.10.007. Epub 2016 Oct 19.

PMID:
27771473
8.

Hemizygous deletion of the HPC-1/syntaxin 1A gene (STX1A) in patients with Williams syndrome.

Nakayama T, Matsuoka R, Kimura M, Hirota H, Mikoshiba K, Shimizu Y, Shimizu N, Akagawa K.

Cytogenet Cell Genet. 1998;82(1-2):49-51.

PMID:
9763659
9.

Autism and Williams syndrome: a case report.

Herguner S, Mukaddes NM.

World J Biol Psychiatry. 2006;7(3):186-8.

PMID:
16861145
10.

Clinical utility of an array comparative genomic hybridization analysis for Williams syndrome.

Yagihashi T, Torii C, Takahashi R, Omori M, Kosaki R, Yoshihashi H, Ihara M, Minagawa-Kawai Y, Yamamoto J, Takahashi T, Kosaki K.

Congenit Anom (Kyoto). 2014 Nov;54(4):225-7. doi: 10.1111/cga.12065.

PMID:
24853877
11.

Anesthesiologic problems in Williams syndrome: the CACNL2A locus is not involved.

Mammi I, Iles DE, Smeets D, Clementi M, Tenconi R.

Hum Genet. 1996 Sep;98(3):317-20.

PMID:
8707301
12.

A novel human gene, WSTF, is deleted in Williams syndrome.

Lu X, Meng X, Morris CA, Keating MT.

Genomics. 1998 Dec 1;54(2):241-9.

PMID:
9828126
13.

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.

PMID:
9003495
14.

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.

15.

Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes.

Meng X, Lu X, Li Z, Green ED, Massa H, Trask BJ, Morris CA, Keating MT.

Hum Genet. 1998 Nov;103(5):590-9.

PMID:
9860302
16.

Comparative mapping of the region of human chromosome 7 deleted in williams syndrome.

DeSilva U, Massa H, Trask BJ, Green ED.

Genome Res. 1999 May;9(5):428-36.

17.

[Williams syndrome: clinical, cytogenetical, neurophysiological and neuroanatomic study].

Aravena T, Castillo S, Carrasco X, Mena I, López J, Rojas JP, Rosemberg C, Schröter C, Aboitiz F.

Rev Med Chil. 2002 Jun;130(6):631-7. Spanish.

PMID:
12194685
18.

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. doi: 10.1159/000439463. Epub 2015 Sep 18.

PMID:
26382598
19.

Renal and urinary findings in 20 patients with Williams-Beuren syndrome diagnosed by fluorescence in situ hybridization (FISH).

Sugayama SM, Koch VH, Furusawa EA, Leone C, Kim CA.

Rev Hosp Clin Fac Med Sao Paulo. 2004 Oct;59(5):266-72. Epub 2004 Oct 29.

20.

"Everybody in the world is my friend" hypersociability in young children with Williams syndrome.

Doyle TF, Bellugi U, Korenberg JR, Graham J.

Am J Med Genet A. 2004 Jan 30;124A(3):263-73.

PMID:
14708099

Supplemental Content

Support Center