Max Planck Publications of Kalscheuer Lab

The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.

Journal Article (3)

Journal Article

Kalscheuer, V. M.; James, V. M.; Himelright, M. L.; Long, P.; Oegema, R.; Jensen, C.; Bienek, M.; Hu, H.; Haas, S. A.; Topf, M. et al.; Hoogeboom, A. J.; Harvey, K.; Walikonis, R.; Harvey, R. J.: Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family. Frontiers in Molecular Neuroscience 8, 8:85 (2016)

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Journal Article

Palmer, E. E.; Leffler, M.; Rogers, C.; Shaw, M.; Carroll, R.; Earl, J.; Cheung, N. W.; Champion, B.; Hu, H.; Haas, S. A. et al.; Kalscheuer, V. M.; Gecz, J.; Field, M.: New insights into Brunner syndrome and potential for targeted therapy. Clinical Genetics: an international journal of genetics in medicine 89 (1), pp. 120 - 127 (2016)

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Journal Article

Williams, L. S.; Kim, H. G.; Kalscheuer, V. M.; Tuck, J. M.; Chorich, L. P.; Sullivan, M. E.; Falkenstrom, A.; Reindollar, R. H.; Layman, L. C.: A balanced chromosomal translocation involving chromosomes 3 and 16 in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome reveals new candidate genes at 3p22.3 and 16p13.3. Molecular Cytogenetics 9, 9:57 (2016)

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