Toomes C - Search Results

1

Inglehearn CF, Yahya S, Smith CEL, Poulter JA, Ali M, Toomes C, Ellingford J, Black GC, Arno G, Webster AR. Inglehearn CF, et al. Among authors: toomes c. Ophthalmology. 2023 Mar;130(3):e9-e10. doi: 10.1016/j.ophtha.2022.10.015. Epub 2022 Nov 15. Ophthalmology. 2023. PMID: 36400608 Free article. No abstract available.

2

Frequent allelic loss and homozygous deletion in chromosome band 8p23 in oral cancer.

Ishwad CS, Shuster M, Bockmühl U, Thakker N, Shah P, Toomes C, Dixon M, Ferrell RE, Gollin SM. Ishwad CS, et al. Among authors: toomes c. Int J Cancer. 1999 Jan 5;80(1):25-31. doi: 10.1002/(sici)1097-0215(19990105)80:1<25::aid-ijc6>3.0.co;2-g. Int J Cancer. 1999. PMID: 9935225 Free article.

3

Molecular cytogenetic evaluation in a patient with a translocation (3;21) associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES).

Praphanphoj V, Goodman BK, Thomas GH, Niel KM, Toomes C, Dixon MJ, Geraghty MT. Praphanphoj V, et al. Among authors: toomes c. Genomics. 2000 Apr 1;65(1):67-9. doi: 10.1006/geno.2000.6157. Genomics. 2000. PMID: 10777667 Free article.

4

The presence of multiple regions of homozygous deletion at the CSMD1 locus in oral squamous cell carcinoma question the role of CSMD1 in head and neck carcinogenesis.

Toomes C, Jackson A, Maguire K, Wood J, Gollin S, Ishwad C, Paterson I, Prime S, Parkinson K, Bell S, Woods G, Markham A, Oliver R, Woodward R, Sloan P, Dixon M, Read A, Thakker N. Toomes C, et al. Genes Chromosomes Cancer. 2003 Jun;37(2):132-40. doi: 10.1002/gcc.10191. Genes Chromosomes Cancer. 2003. PMID: 12696061

5

Coinheritance of two rare genodermatoses (Papillon-Lefèvre syndrome and oculocutaneous albinism type 1) in two families: a genetic study.

Hewitt C, Wu CL, Hattab FN, Amin W, Ghaffar KA, Toomes C, Sloan P, Read AP, James JA, Thakker NS. Hewitt C, et al. Among authors: toomes c. Br J Dermatol. 2004 Dec;151(6):1261-5. doi: 10.1111/j.1365-2133.2004.06237.x. Br J Dermatol. 2004. PMID: 15606524

6

Mitral E wave propagation as an index of left ventricular diastolic function. I: Its hydrodynamic basis.

Pai RG, Yoganathan AP, Toomes C, Eberhardt C, Shah PM. Pai RG, et al. Among authors: toomes c. J Heart Valve Dis. 1998 Jul;7(4):438-44. J Heart Valve Dis. 1998. PMID: 9697068

7

Identification of microcephalin, a protein implicated in determining the size of the human brain.

Jackson AP, Eastwood H, Bell SM, Adu J, Toomes C, Carr IM, Roberts E, Hampshire DJ, Crow YJ, Mighell AJ, Karbani G, Jafri H, Rashid Y, Mueller RF, Markham AF, Woods CG. Jackson AP, et al. Among authors: toomes c. Am J Hum Genet. 2002 Jul;71(1):136-42. doi: 10.1086/341283. Epub 2002 Jun 3. Am J Hum Genet. 2002. PMID: 12046007 Free PMC article.

8

Refinement of a translocation breakpoint associated with blepharophimosis-ptosis-epicanthus inversus syndrome to a 280-kb interval at chromosome 3q23.

Toomes C, Dixon MJ. Toomes C, et al. Genomics. 1998 Nov 1;53(3):308-14. doi: 10.1006/geno.1998.5512. Genomics. 1998. PMID: 9799597

9

Polymorphisms in OPA1 are associated with normal tension glaucoma.

Powell BL, Toomes C, Scott S, Yeung A, Marchbank NJ, Spry PG, Lumb R, Inglehearn CF, Churchill AJ. Powell BL, et al. Among authors: toomes c. Mol Vis. 2003 Sep 22;9:460-4. Mol Vis. 2003. PMID: 14551537 Free article.

10

Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.

Woods CG, Stricker S, Seemann P, Stern R, Cox J, Sherridan E, Roberts E, Springell K, Scott S, Karbani G, Sharif SM, Toomes C, Bond J, Kumar D, Al-Gazali L, Mundlos S. Woods CG, et al. Among authors: toomes c. Am J Hum Genet. 2006 Aug;79(2):402-8. doi: 10.1086/506332. Epub 2006 Jun 23. Am J Hum Genet. 2006. PMID: 16826533 Free PMC article.

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