Latif F - Search Results

1

Microarray based analysis of 3p25-p26 deletions (3p- syndrome).

Shuib S, McMullan D, Rattenberry E, Barber RM, Rahman F, Zatyka M, Chapman C, Macdonald F, Latif F, Davison V, Maher ER. Shuib S, et al. Among authors: latif f. Am J Med Genet A. 2009 Oct;149A(10):2099-105. doi: 10.1002/ajmg.a.32824. Am J Med Genet A. 2009. PMID: 19760623

2

Detailed mapping of a congenital heart disease gene in chromosome 3p25.

Green EK, Priestley MD, Waters J, Maliszewska C, Latif F, Maher ER. Green EK, et al. Among authors: latif f. J Med Genet. 2000 Aug;37(8):581-7. doi: 10.1136/jmg.37.8.581. J Med Genet. 2000. PMID: 10922384 Free PMC article.

3

Copy number profiling in von Hippel-Lindau disease renal cell carcinoma.

Shuib S, Wei W, Sur H, Morris MR, McMullan D, Rattenberry E, Meyer E, Maxwell PH, Kishida T, Yao M, Latif F, Maher ER. Shuib S, et al. Among authors: latif f. Genes Chromosomes Cancer. 2011 Jul;50(7):479-88. doi: 10.1002/gcc.20865. Epub 2011 Mar 31. Genes Chromosomes Cancer. 2011. PMID: 21456047

4

Genetic and functional analysis of the von Hippel-Lindau (VHL) tumour suppressor gene promoter.

Zatyka M, Morrissey C, Kuzmin I, Lerman MI, Latif F, Richards FM, Maher ER. Zatyka M, et al. Among authors: latif f. J Med Genet. 2002 Jul;39(7):463-72. doi: 10.1136/jmg.39.7.463. J Med Genet. 2002. PMID: 12114475 Free PMC article.

5

Analysis of the Birt-Hogg-Dubé (BHD) tumour suppressor gene in sporadic renal cell carcinoma and colorectal cancer.

da Silva NF, Gentle D, Hesson LB, Morton DG, Latif F, Maher ER. da Silva NF, et al. Among authors: latif f. J Med Genet. 2003 Nov;40(11):820-4. doi: 10.1136/jmg.40.11.820. J Med Genet. 2003. PMID: 14627671 Free PMC article.

6

Characterization of a 3;6 translocation associated with renal cell carcinoma.

Foster RE, Abdulrahman M, Morris MR, Prigmore E, Gribble S, Ng B, Gentle D, Ready S, Weston PM, Wiesener MS, Kishida T, Yao M, Davison V, Barbero JL, Chu C, Carter NP, Latif F, Maher ER. Foster RE, et al. Among authors: latif f. Genes Chromosomes Cancer. 2007 Apr;46(4):311-7. doi: 10.1002/gcc.20403. Genes Chromosomes Cancer. 2007. PMID: 17205537 Free PMC article.

7

Familial non-VHL clear cell (conventional) renal cell carcinoma: clinical features, segregation analysis, and mutation analysis of FLCN.

Woodward ER, Ricketts C, Killick P, Gad S, Morris MR, Kavalier F, Hodgson SV, Giraud S, Bressac-de Paillerets B, Chapman C, Escudier B, Latif F, Richard S, Maher ER. Woodward ER, et al. Among authors: latif f. Clin Cancer Res. 2008 Sep 15;14(18):5925-30. doi: 10.1158/1078-0432.CCR-08-0608. Clin Cancer Res. 2008. PMID: 18794106

8

Investigation of the Birt-Hogg-Dube tumour suppressor gene (FLCN) in familial and sporadic colorectal cancer.

Nahorski MS, Lim DH, Martin L, Gille JJ, McKay K, Rehal PK, Ploeger HM, van Steensel M, Tomlinson IP, Latif F, Menko FH, Maher ER. Nahorski MS, et al. Among authors: latif f. J Med Genet. 2010 Jun;47(6):385-90. doi: 10.1136/jmg.2009.073304. J Med Genet. 2010. PMID: 20522427

9

Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility.

Astuti D, Morris MR, Cooper WN, Staals RH, Wake NC, Fews GA, Gill H, Gentle D, Shuib S, Ricketts CJ, Cole T, van Essen AJ, van Lingen RA, Neri G, Opitz JM, Rump P, Stolte-Dijkstra I, Müller F, Pruijn GJ, Latif F, Maher ER. Astuti D, et al. Among authors: latif f. Nat Genet. 2012 Feb 5;44(3):277-84. doi: 10.1038/ng.1071. Nat Genet. 2012. PMID: 22306653

10

Physical mapping of chromosome 3p25-p26 by fluorescence in situ hybridisation (FISH).

Phipps ME, Maher ER, Affara NA, Latif F, Leversha MA, Ferguson-Smith ME, Nakamura Y, Lerman M, Zbar B, Ferguson-Smith MA. Phipps ME, et al. Among authors: latif f. Hum Genet. 1993 Aug;92(1):18-22. doi: 10.1007/BF00216139. Hum Genet. 1993. PMID: 8365722

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