Wadey R - Search Results

1

Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization.

Lindsay EA, Halford S, Wadey R, Scambler PJ, Baldini A. Lindsay EA, et al. Among authors: wadey r. Genomics. 1993 Aug;17(2):403-7. doi: 10.1006/geno.1993.1339. Genomics. 1993. PMID: 8406492

2

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease.

Halford S, Wadey R, Roberts C, Daw SC, Whiting JA, O'Donnell H, Dunham I, Bentley D, Lindsay E, Baldini A, et al. Halford S, et al. Among authors: wadey r. Hum Mol Genet. 1993 Dec;2(12):2099-107. doi: 10.1093/hmg/2.12.2099. Hum Mol Genet. 1993. PMID: 8111380

3

Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134).

Wadey R, Daw S, Wickremasinghe A, Roberts C, Wilson D, Goodship J, Burn J, Halford S, Scambler PJ. Wadey R, et al. J Med Genet. 1993 Oct;30(10):818-21. doi: 10.1136/jmg.30.10.818. J Med Genet. 1993. PMID: 8230156 Free PMC article.

4

Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome.

Sutherland HF, Wadey R, McKie JM, Taylor C, Atif U, Johnstone KA, Halford S, Kim UJ, Goodship J, Baldini A, Scambler PJ. Sutherland HF, et al. Among authors: wadey r. Am J Hum Genet. 1996 Jul;59(1):23-31. Am J Hum Genet. 1996. PMID: 8659529 Free PMC article.

5

Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome.

Carey AH, Kelly D, Halford S, Wadey R, Wilson D, Goodship J, Burn J, Paul T, Sharkey A, Dumanski J, et al. Carey AH, et al. Among authors: wadey r. Am J Hum Genet. 1992 Nov;51(5):964-70. Am J Hum Genet. 1992. PMID: 1415265 Free PMC article.

6

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

Burn J, Takao A, Wilson D, Cross I, Momma K, Wadey R, Scambler P, Goodship J. Burn J, et al. Among authors: wadey r. J Med Genet. 1993 Oct;30(10):822-4. doi: 10.1136/jmg.30.10.822. J Med Genet. 1993. PMID: 8230157 Free PMC article.

7

Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome.

Halford S, Wilson DI, Daw SC, Roberts C, Wadey R, Kamath S, Wickremasinghe A, Burn J, Goodship J, Mattei MG, et al. Halford S, et al. Among authors: wadey r. Hum Mol Genet. 1993 Oct;2(10):1577-82. doi: 10.1093/hmg/2.10.1577. Hum Mol Genet. 1993. PMID: 8268909

8

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.

Carlson C, Sirotkin H, Pandita R, Goldberg R, McKie J, Wadey R, Patanjali SR, Weissman SM, Anyane-Yeboa K, Warburton D, Scambler P, Shprintzen R, Kucherlapati R, Morrow BE. Carlson C, et al. Among authors: wadey r. Am J Hum Genet. 1997 Sep;61(3):620-9. doi: 10.1086/515508. Am J Hum Genet. 1997. PMID: 9326327 Free PMC article.

9

Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome.

Wadey R, Daw S, Taylor C, Atif U, Kamath S, Halford S, O'Donnell H, Wilson D, Goodship J, Burn J, et al. Wadey R, et al. Hum Mol Genet. 1995 Jun;4(6):1027-33. doi: 10.1093/hmg/4.6.1027. Hum Mol Genet. 1995. PMID: 7655455

10

Direct selection of conserved cDNAs from the DiGeorge critical region: isolation of a novel CDC45-like gene.

McKie JM, Wadey RB, Sutherland HF, Taylor CL, Scambler PJ. McKie JM, et al. Among authors: wadey rb. Genome Res. 1998 Aug;8(8):834-41. doi: 10.1101/gr.8.8.834. Genome Res. 1998. PMID: 9724329 Free PMC article.

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