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There are 519313 results for: content related to: Epigenetics of colorectal cancer

  1. Epigenetic and genetic disturbance of the imprinted 11p15 region in Beckwith–Wiedemann and Silver–Russell syndromes

    Clinical Genetics

    Volume 81, Issue 4, April 2012, Pages: 350–361, J Demars and C Gicquel

    Article first published online : 16 JAN 2012, DOI: 10.1111/j.1399-0004.2011.01822.x

  2. Chimera and other fertilization errors

    Clinical Genetics

    Volume 70, Issue 5, November 2006, Pages: 363–373, V Malan, M Vekemans and C Turleau

    Article first published online : 14 SEP 2006, DOI: 10.1111/j.1399-0004.2006.00689.x

  3. A genome-wide linkage scan for iron phenotype quantitative trait loci: the HEIRS Family Study

    Clinical Genetics

    Volume 71, Issue 6, June 2007, Pages: 518–529, RT Acton, BM Snively, JC Barton, CE McLaren, PC Adams, SS Rich, JH Eckfeldt, RD Press, P Sholinsky, C Leiendecker-Foster, GD McLaren, MR Speechley, EL Harris, FW Dawkins, VR Gordeuk and the Hemochromatosis and Iron Overload Screening Study Research Investigators

    Article first published online : 9 MAY 2007, DOI: 10.1111/j.1399-0004.2007.00804.x

  4. Genetic epidemiology of alpha-1 antitrypsin deficiency in southern Europe: France, Italy, Portugal and Spain

    Clinical Genetics

    Volume 63, Issue 6, June 2003, Pages: 490–509, FJ De Serres, I Blanco and E Fernández-Bustillo

    Article first published online : 3 JUN 2003, DOI: 10.1034/j.1399-0004.2003.00078.x

  5. X-linked mental retardation: further lumping, splitting and emerging phenotypes

    Clinical Genetics

    Volume 67, Issue 6, June 2005, Pages: 451–467, T Kleefstra and BCJ Hamel

    Article first published online : 31 MAR 2005, DOI: 10.1111/j.1399-0004.2005.00434.x

  6. Fishing for new genes in skin biology: impact of cytogenetics on gene discovery

    Clinical Genetics

    Volume 66, Issue 2, August 2004, Pages: 94–106, M Tadin-Strapps, D Warburton, JC Salas-Alanis, LD Lopez-Cepeda and AM Christiano

    Article first published online : 14 JUL 2004, DOI: 10.1111/j.0009-9163.2004.00301.x

  7. Toward understanding the genetic basis of neural tube defects

    Clinical Genetics

    Volume 71, Issue 4, April 2007, Pages: 295–310, Z Kibar, V Capra and P Gros

    Article first published online : 25 APR 2007, DOI: 10.1111/j.1399-0004.2007.00793.x

  8. The early-life social environment and DNA methylation

    Clinical Genetics

    Volume 81, Issue 4, April 2012, Pages: 341–349, M Szyf

    Article first published online : 13 FEB 2012, DOI: 10.1111/j.1399-0004.2012.01843.x

  9. Advances in the detection of chromosomal aberrations using spectral karyotyping

    Clinical Genetics

    Volume 59, Issue 2, February 2001, Pages: 65–73, J Bayani and JA Squire

    Article first published online : 20 DEC 2001, DOI: 10.1034/j.1399-0004.2001.590201.x

  10. The causes and consequences of random and non-random X chromosome inactivation in humans

    Clinical Genetics

    Volume 58, Issue 5, November 2000, Pages: 353–363, CJ Brown and WP Robinson

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.2000.580504.x

  11. What monozygotic twins discordant for phenotype illustrate about mechanisms influencing genetic forms of neurodegeneration

    Clinical Genetics

    Volume 81, Issue 4, April 2012, Pages: 325–333, ME Ketelaar, RMW Hofstra and MR Hayden

    Article first published online : 12 NOV 2011, DOI: 10.1111/j.1399-0004.2011.01795.x

  12. Kabuki syndrome: a review

    Clinical Genetics

    Volume 67, Issue 3, March 2005, Pages: 209–219, MP Adam and L Hudgins

    Article first published online : 20 OCT 2004, DOI: 10.1111/j.1399-0004.2004.00348.x

  13. Stüve–Wiedemann syndrome and related bent bone dysplasias

    Clinical Genetics

    Volume 82, Issue 1, July 2012, Pages: 12–21, N A Akawi, B R Ali and L Al-Gazali

    Article first published online : 21 FEB 2012, DOI: 10.1111/j.1399-0004.2012.01852.x

  14. CYP21 mutations and congenital adrenal hyperplasia

    Clinical Genetics

    Volume 59, Issue 5, May 2001, Pages: 293–301, HH Lee

    Article first published online : 12 JAN 2002, DOI: 10.1034/j.1399-0004.2001.590501.x

  15. Increased release and activity of matrix metalloproteinase-9 in patients with mandibuloacral dysplasia type A, a rare premature ageing syndrome

    Clinical Genetics

    Volume 74, Issue 4, October 2008, Pages: 374–383, F Lombardi, GF Fasciglione, MR D’Apice, A Vielle, M D’Adamo, P Sbraccia, S Marini, P Borgiani, M Coletta and G Novelli

    Article first published online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.2008.01034.x

  16. Neurodevelopmental consequences of maternal distress: what do we really know?

    Clinical Genetics

    Volume 83, Issue 2, February 2013, Pages: 108–117, C Schuurmans and DM Kurrasch

    Article first published online : 6 DEC 2012, DOI: 10.1111/cge.12049

  17. Ciliary dysfunction and obesity

    Clinical Genetics

    Volume 77, Issue 1, January 2010, Pages: 18–27, CA Mok, E Héon and M Zhen

    Article first published online : 23 NOV 2009, DOI: 10.1111/j.1399-0004.2009.01305.x

  18. CGG repeat in the FMR1 gene: size matters

    Clinical Genetics

    Volume 80, Issue 3, September 2011, Pages: 214–225, R Willemsen, J Levenga and BA Oostra

    Article first published online : 30 JUN 2011, DOI: 10.1111/j.1399-0004.2011.01723.x

  19. Inherited disorders of cholesterol biosynthesis

    Clinical Genetics

    Volume 61, Issue 6, June 2002, Pages: 393–403, HR Waterham

    Article first published online : 11 JUL 2002, DOI: 10.1034/j.1399-0004.2002.610601.x

  20. Claudins: unlocking the code to tight junction function during embryogenesis and in disease

    Clinical Genetics

    Volume 77, Issue 4, April 2010, Pages: 314–325, IR Gupta and AK Ryan

    Article first published online : 17 FEB 2010, DOI: 10.1111/j.1399-0004.2010.01397.x