Similar articles for PMID: 12838549

Year	Number of Results
1989	1
1995	5
1996	10
1997	7
1998	13
1999	8
2000	8
2001	2
2002	3
2003	5
2004	1
2005	3
2006	4
2007	3
2008	1
2009	3
2010	3
2011	1
2012	1
2013	2
2014	3
2015	1
2016	2
2017	2
2018	3
2019	4
2020	2
2022	1
2023	1
2024	0

1

Heat shock protein 27 gene: chromosomal and molecular location and relationship to Williams syndrome.

Stock AD, Spallone PA, Dennis TR, Netski D, Morris CA, Mervis CB, Hobart HH. Stock AD, et al. Am J Med Genet A. 2003 Jul 30;120A(3):320-5. doi: 10.1002/ajmg.a.20055. Am J Med Genet A. 2003. PMID: 12838549

2

A complete physical contig and partial transcript map of the Williams syndrome critical region.

Hockenhull EL, Carette MJ, Metcalfe K, Donnai D, Read AP, Tassabehji M. Hockenhull EL, et al. Genomics. 1999 Jun 1;58(2):138-45. doi: 10.1006/geno.1999.5815. Genomics. 1999. PMID: 10366445

3

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

DeSilva U, Massa H, Trask BJ, Green ED. DeSilva U, et al. Genome Res. 1999 May;9(5):428-36. Genome Res. 1999. PMID: 10330122 Free PMC article.

4

Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth.

Pérez Jurado LA, Peoples R, Kaplan P, Hamel BC, Francke U. Pérez Jurado LA, et al. Am J Hum Genet. 1996 Oct;59(4):781-92. Am J Hum Genet. 1996. PMID: 8808592 Free PMC article.

5

VI. Genome structure and cognitive map of Williams syndrome.

Korenberg JR, Chen XN, Hirota H, Lai Z, Bellugi U, Burian D, Roe B, Matsuoka R. Korenberg JR, et al. J Cogn Neurosci. 2000;12 Suppl 1:89-107. doi: 10.1162/089892900562002. J Cogn Neurosci. 2000. PMID: 10953236 Clinical Trial.

6

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. Meng X, et al. Hum Genet. 1998 Nov;103(5):590-9. doi: 10.1007/s004390050874. Hum Genet. 1998. PMID: 9860302

7

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. Brøndum-Nielsen K, et al. Hum Genet. 1997 Jan;99(1):56-61. doi: 10.1007/s004390050311. Hum Genet. 1997. PMID: 9003495

8

Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin.

Wu YQ, Sutton VR, Nickerson E, Lupski JR, Potocki L, Korenberg JR, Greenberg F, Tassabehji M, Shaffer LG. Wu YQ, et al. Am J Med Genet. 1998 Jun 16;78(1):82-9. doi: 10.1002/(sici)1096-8628(19980616)78:1<82::aid-ajmg17>3.0.co;2-k. Am J Med Genet. 1998. PMID: 9637430

9

Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23.

Hirota H, Matsuoka R, Chen XN, Salandanan LS, Lincoln A, Rose FE, Sunahara M, Osawa M, Bellugi U, Korenberg JR. Hirota H, et al. Genet Med. 2003 Jul-Aug;5(4):311-21. doi: 10.1097/01.GIM.0000076975.10224.67. Genet Med. 2003. PMID: 12865760

10

Comparing two diagnostic laboratory tests for Williams syndrome: fluorescent in situ hybridization versus multiplex ligation-dependent probe amplification.

van Hagen JM, Eussen HJ, van Schooten R, van Der Geest JN, Lagers-van Haselen GC, Wouters CH, De Zeeuw CI, Gille JJ. van Hagen JM, et al. Genet Test. 2007 Fall;11(3):321-7. doi: 10.1089/gte.2007.0007. Genet Test. 2007. PMID: 17949295

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