1. Alberts, B., Johnson, A., Lewis, J., Raff, M., Roberts, K., & Walter, P. (2008). Molecular biology of the cell. (5 ed.). New York, NY: Garland Science, Taylor & Francis Group, LLC.
2. Alpha thalassemia . (2014). Retrieved from http://ghr.nlm.nih.gov/condition/alpha-thalassemia.
3. Bickmore, W. A., & van der Maarel, S. M. (2003). Perturbations of chromatin structure in human genetic disease: recent advances. Human Molecular Genetics, 12(2), 207-213.Dupont, C., Guimiot, F., Perrin, L., Marey, I., Smiljkovski, D., Le Tessier, D., Lebugle, C., Baumann, C., Bourdoncle, P., Tabet, A. C., Aboura, A., Benzacken, B., & Dupont, J. M. (2012). 3d position of pericentromeric heterochromatin within the nucleus of a patient with icf syndrome. Clinical Genetics, 82, 187-192.
4. Dupont, C., Guimiot, F., Perrin, L., Marey, I., Smiljkovski, D., Le Tessier, D., Lebugle, C., Baumann, C., Bourdoncle, P., Tabet, A. C., Aboura, A., Benzacken, B., & Dupont, J. M. (2012). 3d position of pericentromeric heterochromatin within the nucleus of a patient with icf syndrome. Clinical Genetics, 82, 187-192.
5. Hendrich, B., & Bickmore, W. H. (2001). Human diseases with underlying defects in chromatin structure and modification. Human Molecular Genetics, 10(20), 2233-2242.
6. Information about fshd. Retrieved March 12, 2014 from: http://www.fshsociety.org/pages/abtWhat.html
7. Iourov, I. Y., Vorsanova, S. G., Voinova, V. Y., Kurinnaia, O. S., Zelenova, M. A., Demidova, I. A., & Yurov, Y. B. (2012). Xq28 (mecp2) microdeletions are common in mutation-negative females with rett syndrome and cause mild subtypes of the disease. BioMed Central, 1-18.
8. Lana, E., Megarbane, A., Tourriere, H., Sarda, P., Lefranc, G., Claustres, M., & De Sario, A. (2012). dna replication is altered in immunodeficiency centromeric instability facial anomalies (icf) cells carrying dnmt3b mutations. European Journal of Human Genetics, 20, 1044-1050.
9. National Library of Medicine (US). Genetics Home Reference. Bethesda, MD. The Library; 2014 March 4. Coffin-Lowry syndrome. Retrieved March 12, 2014 from: http://ghr.nlm.nih.gov/condition/coffin-lowry-syndrome.
10. Pirozhkova1, I., Petrov, A., Dmitriev, P., Laoudj, D., Lipinski, M. A., & Vassetzky, Y. (2008). A functional role for 4qa/b in the structural rearrangement of the 4q35 region and in the regulation of frg1 and ant1 in facioscapulohumeral dystrophy. PLoS ONE, 3(10), 1-9.
11. Poole, R. L., Leith, D. J., Docherty, L. E., Shmela, M. E., Gicquel, C., Splitt, M., Temple, K. I., & Mackay, D. J. G. (2012). Beckwith–wiedemann syndrome caused by maternally inherited mutation of an oct-binding motif in the igf2/h19-imprinting control region, icr1. European Journal of Human Genetics, 20, 240-243.
12. Yasui, D. H., Xu, H., Dunaway, K. W., LaSalle, J. M., Jin, L., & Maezawa, I. (2013). Mecp2 modulates gene expression pathways in astrocytes. Molecular Autism, 4(3), 1-11.
13. Zhou, Z., Hong, E. J., Cohen, S., Zhao, W. N., Ho, H. Y., Schmidt, L., Chen, W.G., Lin, Y., Savner, E., Griffith, E.C., Hu, L., Steen, J.A., Weitz, C.J., & Greenberg, M. E. (2006). Brain-specific phosphorylation of mecp2 regulates activity-dependent bdnf transcription, dendritic growth, and spine maturation. Neuron, 52(2), 255-269.
2. Alpha thalassemia . (2014). Retrieved from http://ghr.nlm.nih.gov/condition/alpha-thalassemia.
3. Bickmore, W. A., & van der Maarel, S. M. (2003). Perturbations of chromatin structure in human genetic disease: recent advances. Human Molecular Genetics, 12(2), 207-213.Dupont, C., Guimiot, F., Perrin, L., Marey, I., Smiljkovski, D., Le Tessier, D., Lebugle, C., Baumann, C., Bourdoncle, P., Tabet, A. C., Aboura, A., Benzacken, B., & Dupont, J. M. (2012). 3d position of pericentromeric heterochromatin within the nucleus of a patient with icf syndrome. Clinical Genetics, 82, 187-192.
4. Dupont, C., Guimiot, F., Perrin, L., Marey, I., Smiljkovski, D., Le Tessier, D., Lebugle, C., Baumann, C., Bourdoncle, P., Tabet, A. C., Aboura, A., Benzacken, B., & Dupont, J. M. (2012). 3d position of pericentromeric heterochromatin within the nucleus of a patient with icf syndrome. Clinical Genetics, 82, 187-192.
5. Hendrich, B., & Bickmore, W. H. (2001). Human diseases with underlying defects in chromatin structure and modification. Human Molecular Genetics, 10(20), 2233-2242.
6. Information about fshd. Retrieved March 12, 2014 from: http://www.fshsociety.org/pages/abtWhat.html
7. Iourov, I. Y., Vorsanova, S. G., Voinova, V. Y., Kurinnaia, O. S., Zelenova, M. A., Demidova, I. A., & Yurov, Y. B. (2012). Xq28 (mecp2) microdeletions are common in mutation-negative females with rett syndrome and cause mild subtypes of the disease. BioMed Central, 1-18.
8. Lana, E., Megarbane, A., Tourriere, H., Sarda, P., Lefranc, G., Claustres, M., & De Sario, A. (2012). dna replication is altered in immunodeficiency centromeric instability facial anomalies (icf) cells carrying dnmt3b mutations. European Journal of Human Genetics, 20, 1044-1050.
9. National Library of Medicine (US). Genetics Home Reference. Bethesda, MD. The Library; 2014 March 4. Coffin-Lowry syndrome. Retrieved March 12, 2014 from: http://ghr.nlm.nih.gov/condition/coffin-lowry-syndrome.
10. Pirozhkova1, I., Petrov, A., Dmitriev, P., Laoudj, D., Lipinski, M. A., & Vassetzky, Y. (2008). A functional role for 4qa/b in the structural rearrangement of the 4q35 region and in the regulation of frg1 and ant1 in facioscapulohumeral dystrophy. PLoS ONE, 3(10), 1-9.
11. Poole, R. L., Leith, D. J., Docherty, L. E., Shmela, M. E., Gicquel, C., Splitt, M., Temple, K. I., & Mackay, D. J. G. (2012). Beckwith–wiedemann syndrome caused by maternally inherited mutation of an oct-binding motif in the igf2/h19-imprinting control region, icr1. European Journal of Human Genetics, 20, 240-243.
12. Yasui, D. H., Xu, H., Dunaway, K. W., LaSalle, J. M., Jin, L., & Maezawa, I. (2013). Mecp2 modulates gene expression pathways in astrocytes. Molecular Autism, 4(3), 1-11.
13. Zhou, Z., Hong, E. J., Cohen, S., Zhao, W. N., Ho, H. Y., Schmidt, L., Chen, W.G., Lin, Y., Savner, E., Griffith, E.C., Hu, L., Steen, J.A., Weitz, C.J., & Greenberg, M. E. (2006). Brain-specific phosphorylation of mecp2 regulates activity-dependent bdnf transcription, dendritic growth, and spine maturation. Neuron, 52(2), 255-269.
Edited by Cheryl Ann Fleming and Ashley Lauren McPhee