Publikationen von H.-G. Kim
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Zeitschriftenartikel (3)
1.
Zeitschriftenartikel
S. Minocherhomji, C. Hansen, H.-G. Kim, Y. Mang, M. Bak, P. Guldberg, N. Papadopoulos, H. Eiberg, G. D. Doh, K. Møllgard, J. M. Hertz, J. E. Nielsen, H.-H. Ropers, Z. Tumer, N. Tommerup, V. M. Kalscheuer, and A. Silahtaroglu, "Epigenetic remodelling and dysregulation of DLGAP4 is linked with early-onset cerebellar ataxia," Human Molecular Genetics 23 (23), 6163-6176 (2014).
2.
Zeitschriftenartikel
K. R. Jun, R. Ullmann, S. Khan, L. C. Layman, and H.-G. Kim, "Interstitial microduplication at 2p11.2 in a patient with syndromic intellectual disability: 30-year follow-up," Molecular Cytogenetics 2014, 7:52 (2014).
3.
Zeitschriftenartikel
H.-G. Kim, H. T. Kim, N. T. Leach, F. Lan, R. Ullmann, A. Silahtaroglu, I. Kurth, A. Nowka, I. S. Seong, Y. Shen, M. E. Talkowski, D. Ruderfer, J. H. Lee, C. Glotzbach, K. Ha, S. Kjaergaard, A. V. Levin, B. F. Romeike, T. Kleefstra, O. Bartsch, S. H. Elsea, E. W. Jabs, M. E. Macdonald, D. J. Harris, B. J. Quade, H.-H. Ropers, L. G. Shaffer, K. Kutsche, L. C. Layman, N. Tommerup, V. M. Kalscheuer, Y. Shi, C. C. Morton, C. H. Kim, and J. F. Gusella, "Translocations Disrupting PHF21A in the Potocki-Shaffer-Syndrome Region Are Associated with Intellectual Disability and Craniofacial Anomalies," The American Journal of Human Genetics 91 (1), 56-72 (2012).