Wadey R - Search Results

1

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.

2

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.

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

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

5

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

6

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.

7

A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.

Ross AJ, Ruiz-Perez V, Wang Y, Hagan DM, Scherer S, Lynch SA, Lindsay S, Custard E, Belloni E, Wilson DI, Wadey R, Goodman F, Orstavik KH, Monclair T, Robson S, Reardon W, Burn J, Scambler P, Strachan T. Ross AJ, et al. Among authors: wadey r. Nat Genet. 1998 Dec;20(4):358-61. doi: 10.1038/3828. Nat Genet. 1998. PMID: 9843207

8

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

9

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.

10

Possible role for COMT in psychosis associated with velo-cardio-facial syndrome.

Dunham I, Collins J, Wadey R, Scambler P. Dunham I, et al. Among authors: wadey r. Lancet. 1992 Nov 28;340(8831):1361-2. doi: 10.1016/0140-6736(92)92553-r. Lancet. 1992. PMID: 1360084 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

53 results

Search Page

Filters