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Items: 1 to 20 of 168

1.

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
2.

A novel human gene FKBP6 is deleted in Williams syndrome.

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

Genomics. 1998 Sep 1;52(2):130-7.

PMID:
9782077
3.

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
4.

Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome.

Osborne LR, Campbell T, Daradich A, Scherer SW, Tsui LC.

Genomics. 1999 Apr 15;57(2):279-84.

PMID:
10198167
5.

Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients.

Osborne LR, Martindale D, Scherer SW, Shi XM, Huizenga J, Heng HH, Costa T, Pober B, Lew L, Brinkman J, Rommens J, Koop B, Tsui LC.

Genomics. 1996 Sep 1;36(2):328-36.

PMID:
8812460
6.

A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndrome.

Tassabehji M, Carette M, Wilmot C, Donnai D, Read AP, Metcalfe K.

Eur J Hum Genet. 1999 Oct-Nov;7(7):737-47.

7.

Identification of the WBSCR9 gene, encoding a novel transcriptional regulator, in the Williams-Beuren syndrome deletion at 7q11.23.

Peoples RJ, Cisco MJ, Kaplan P, Francke U.

Cytogenet Cell Genet. 1998;82(3-4):238-46.

PMID:
9858827
9.

Cloning and developmental expression of WSTF during Xenopus laevis embryogenesis.

Cus R, Maurus D, Kühl M.

Gene Expr Patterns. 2006 Apr;6(4):340-6. Epub 2006 Jan 30.

PMID:
16448863
10.

The murine CYLN2 gene: genomic organization, chromosome localization, and comparison to the human gene that is located within the 7q11.23 Williams syndrome critical region.

Hoogenraad CC, Eussen BH, Langeveld A, van Haperen R, Winterberg S, Wouters CH, Grosveld F, De Zeeuw CI, Galjart N.

Genomics. 1998 Nov 1;53(3):348-58.

PMID:
9799601
11.
12.

Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit.

Berti L, Mittler G, Przemeck GK, Stelzer G, Günzler B, Amati F, Conti E, Dallapiccola B, Hrabé de Angelis M, Novelli G, Meisterernst M.

Genomics. 2001 Jun 15;74(3):320-32.

PMID:
11414760
13.

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 11;224(1-2):35-44.

PMID:
9931421
14.

A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23.

Wang YK, Samos CH, Peoples R, Pérez-Jurado LA, Nusse R, Francke U.

Hum Mol Genet. 1997 Mar;6(3):465-72.

15.
16.

Identification of GTF2IRD1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23.

Franke Y, Peoples RJ, Francke U.

Cytogenet Cell Genet. 1999;86(3-4):296-304.

PMID:
10575229
17.

Identification, characterization and mapping of the human ZIS (zinc-finger, splicing) gene.

Nakano M, Yoshiura K, Oikawa M, Miyoshi O, Yamada K, Kondo S, Miwa N, Soeda E, Jinno Y, Fujii T, Niikawa N.

Gene. 1998 Dec 28;225(1-2):59-65.

PMID:
9931435
18.
19.
20.

Identification of additional transcripts in the Williams-Beuren syndrome critical region.

Merla G, Ucla C, Guipponi M, Reymond A.

Hum Genet. 2002 May;110(5):429-38. Epub 2002 Mar 28.

PMID:
12073013
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