Wright TJ - Search Results

1

"Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype.

Zollino M, Wright TJ, Di Stefano C, Tosolini A, Battaglia A, Altherr MR, Neri G. Zollino M, et al. Among authors: wright tj. Am J Med Genet. 1999 Feb 19;82(5):371-5. Am J Med Genet. 1999. PMID: 10069706

2

A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region.

Wright TJ, Ricke DO, Denison K, Abmayr S, Cotter PD, Hirschhorn K, Keinänen M, McDonald-McGinn D, Somer M, Spinner N, Yang-Feng T, Zackai E, Altherr MR. Wright TJ, et al. Hum Mol Genet. 1997 Feb;6(2):317-24. doi: 10.1093/hmg/6.2.317. Hum Mol Genet. 1997. PMID: 9063753

3

Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35.

van Deutekom JC, Lemmers RJ, Grewal PK, van Geel M, Romberg S, Dauwerse HG, Wright TJ, Padberg GW, Hofker MH, Hewitt JE, Frants RR. van Deutekom JC, et al. Among authors: wright tj. Hum Mol Genet. 1996 May;5(5):581-90. doi: 10.1093/hmg/5.5.581. Hum Mol Genet. 1996. PMID: 8733123

4

Wolf-Hirschhorn (4p-) syndrome.

Battaglia A, Carey JC, Wright TJ. Battaglia A, et al. Among authors: wright tj. Adv Pediatr. 2001;48:75-113. Adv Pediatr. 2001. PMID: 11480768 Review.

5

Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome.

Zollino M, Di Stefano C, Zampino G, Mastroiacovo P, Wright TJ, Sorge G, Selicorni A, Tenconi R, Zappalà A, Battaglia A, Di Rocco M, Palka G, Pallotta R, Altherr MR, Neri G. Zollino M, et al. Among authors: wright tj. Am J Med Genet. 2000 Sep 18;94(3):254-61. doi: 10.1002/1096-8628(20000918)94:3<254::aid-ajmg13>3.0.co;2-7. Am J Med Genet. 2000. PMID: 10995514

6

Comparative analysis of a novel gene from the Wolf-Hirschhorn/Pitt-Rogers-Danks syndrome critical region.

Wright TJ, Costa JL, Naranjo C, Francis-West P, Altherr MR. Wright TJ, et al. Genomics. 1999 Jul 15;59(2):203-12. doi: 10.1006/geno.1999.5871. Genomics. 1999. PMID: 10409432

7

WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma.

Stec I, Wright TJ, van Ommen GJ, de Boer PA, van Haeringen A, Moorman AF, Altherr MR, den Dunnen JT. Stec I, et al. Among authors: wright tj. Hum Mol Genet. 1998 Jul;7(7):1071-82. doi: 10.1093/hmg/7.7.1071. Hum Mol Genet. 1998. PMID: 9618163

8

Wolf-Hirschhorn and Pitt-Rogers-Danks syndromes caused by overlapping 4p deletions.

Wright TJ, Clemens M, Quarrell O, Altherr MR. Wright TJ, et al. Am J Med Genet. 1998 Feb 3;75(4):345-50. doi: 10.1002/(sici)1096-8628(19980203)75:4<345::aid-ajmg2>3.0.co;2-p. Am J Med Genet. 1998. PMID: 9482639

9

Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairs.

Altherr MR, Wright TJ, Denison K, Perez-Castro AV, Johnson VP. Altherr MR, et al. Among authors: wright tj. Am J Med Genet. 1997 Jul 11;71(1):47-53. doi: 10.1002/(sici)1096-8628(19970711)71:1<47::aid-ajmg9>3.0.co;2-n. Am J Med Genet. 1997. PMID: 9215768

10

High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.

Fang YY, Bain S, Haan EA, Eyre HJ, MacDonald M, Wright TJ, Altherr MR, Riess O, Sutherland G, Callen DF. Fang YY, et al. Among authors: wright tj. Am J Med Genet. 1997 Sep 5;71(4):453-7. Am J Med Genet. 1997. PMID: 9286454

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