Results of search for 'au:"MAHER, E"' › مکتبة رقمیه للعلوم الطبيه catalog

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	301.	Achromatopsia caused by novel mutations in both CNGA3 and CNGB3. [electronic resource] by Johnson, S Michaelides, M Aligianis, I A Ainsworth, J R Mollon, J D Maher, E R Moore, A T Hunt, D M Producer: 20040223 In: Journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	302.	Electromagnetic and Thermal Simulations of Human Neurons for SAR Applications. [electronic resource] by Perez, Felipe Millholland, Gilbert Peddinti, Seshasai Vamsi Krishna Thella, Ashok Kumar Rizkalla, James Salama, Paul Rizkalla, Maher Morisaki, Jorge Rizkalla, Maher E Publication details: Journal of biomedical science and engineering Aug 2016 In: Journal of biomedical science and engineering vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	303.	Suction vs water seal after pulmonary resection: a randomized prospective study. [electronic resource] by Marshall, M Blair Deeb, Maher E Bleier, Joshua I S Kucharczuk, John C Friedberg, Joseph S Kaiser, Larry R Shrager, Joseph B Producer: 20020409 In: Chest vol. 121 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	304.	Genomic organization and chromosomal localization of the human CUL2 gene and the role of von Hippel-Lindau tumor suppressor-binding protein (CUL2 and VBP1) mutation and loss in renal-cell carcinoma development. [electronic resource] by Clifford, S C Walsh, S Hewson, K Green, E K Brinke, A Green, P M Gianelli, F Eng, C Maher, E R Producer: 19990827 In: Genes, chromosomes & cancer vol. 26 Availability: No items available. Save to lists Add to cart (remove)
	305.	Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the alpha-subunit of cone specific transducin (GNAT2). [electronic resource] by Michaelides, M Aligianis, I A Holder, G E Simunovic, M Mollon, J D Maher, E R Hunt, D M Moore, A T Producer: 20040126 In: The British journal of ophthalmology vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	306.	Identification of candidate tumour suppressor genes frequently methylated in renal cell carcinoma. [electronic resource] by Morris, M R Ricketts, C Gentle, D Abdulrahman, M Clarke, N Brown, M Kishida, T Yao, M Latif, F Maher, E R Producer: 20100505 In: Oncogene vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	307.	von Hippel-Lindau disease: identification of deletion mutations by pulsed-field gel electrophoresis. [electronic resource] by Yao, M Latif, F Orcutt, M L Kuzmin, I Stackhouse, T Zhou, F W Tory, K Duh, F M Richards, F Maher, E Producer: 19940121 In: Human genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	308.	Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II. [electronic resource] by Neumann, H P Eng, C Mulligan, L M Glavac, D Zäuner, I Ponder, B A Crossey, P A Maher, E R Brauch, H Producer: 19951031 In: JAMA vol. 274 Availability: No items available. Save to lists Add to cart (remove)
	309.	Germline SDHD mutation in familial phaeochromocytoma. [electronic resource] by Astuti, D Douglas, F Lennard, T W Aligianis, I A Woodward, E R Evans, D G Eng, C Latif, F Maher, E R Producer: 20010607 In: Lancet (London, England) vol. 357 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	310.	Functional epigenomics approach to identify methylated candidate tumour suppressor genes in renal cell carcinoma. [electronic resource] by Morris, M R Gentle, D Abdulrahman, M Clarke, N Brown, M Kishida, T Yao, M Teh, B T Latif, F Maher, E R Producer: 20080327 In: British journal of cancer vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	311.	Regulation of Igf2 imprinting in development and disease. [electronic resource] by Reik, W Bowden, L Constancia, M Dean, W Feil, R Forné, T Kelsey, G Maher, E Moore, T Sun, F L Walter, J Producer: 19970506 In: The International journal of developmental biology vol. Suppl 1 Availability: No items available. Save to lists Add to cart (remove)
	312.	A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis. [electronic resource] by Walsh, D M Shah, S H Simpson, M A Morgan, N V Khaliq, S Trembath, R C Mehdi, S Q Maher, E R Producer: 20131126 In: Scientifica vol. 2012 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	313.	Frequent 3p allele loss and epigenetic inactivation of the RASSF1A tumour suppressor gene from region 3p21.3 in head and neck squamous cell carcinoma. [electronic resource] by Hogg, R P Honorio, S Martinez, A Agathanggelou, A Dallol, A Fullwood, P Weichselbaum, R Kuo, M J Maher, E R Latif, F Producer: 20021001 In: European journal of cancer (Oxford, England : 1990) vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	314.	Detailed genetic and physical mapping of tumor suppressor loci on chromosome 3p in ovarian cancer. [electronic resource] by Fullwood, P Marchini, S Rader, J S Martinez, A Macartney, D Broggini, M Morelli, C Barbanti-Brodano, G Maher, E R Latif, F Producer: 19991008 In: Cancer research vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	315.	Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. [electronic resource] by Astuti, D Latif, F Dallol, A Dahia, P L Douglas, F George, E Sköldberg, F Husebye, E S Eng, C Maher, E R Producer: 20010802 In: American journal of human genetics vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	316.	Pregnancy and perinatal outcomes after assisted reproduction: a comparative study. [electronic resource] by Allen, C Bowdin, S Harrison, R F Sutcliffe, A G Brueton, L Kirby, G Kirkman-Brown, J Barrett, C Reardon, W Maher, E Producer: 20081009 In: Irish journal of medical science vol. 177 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	317.	Analysis of multiple renal cell adenomas and carcinomas suggests allelic loss at 3p21 to be a prerequisite for malignant development. [electronic resource] by van den Berg, A Dijkhuizen, T Draaijers, T G Hulsbeek, M M Maher, E R van den Berg, E Störkel, S Buys, C H Producer: 19970924 In: Genes, chromosomes & cancer vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	318.	Contrasting effects on HIF-1alpha regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau disease. [electronic resource] by Clifford, S C Cockman, M E Smallwood, A C Mole, D R Woodward, E R Maxwell, P H Ratcliffe, P J Maher, E R Producer: 20010712 In: Human molecular genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	319.	Von Hippel-Lindau disease: a genetic study. [electronic resource] by Maher, E R Iselius, L Yates, J R Littler, M Benjamin, C Harris, R Sampson, J Williams, A Ferguson-Smith, M A Morton, N Producer: 19911021 In: Journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	320.	Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2). [electronic resource] by Aligianis, I A Forshew, T Johnson, S Michaelides, M Johnson, C A Trembath, R C Hunt, D M Moore, A T Maher, E R Producer: 20021112 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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