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Zeitschriftenartikel (4)

1.
Zeitschriftenartikel
Tzschach, A.; Ullmann, R.; Ahmed, A.; Martin, T.; Weber, G.; Decker-Schwering, O.; Pauly, F.; Shamdeen, M. G.; Reith, W.; Oehl-Jaschkowitz, B.: Christianson syndrome in a patient with an interstitial Xq26.3 deletion. Am J Med Genet A 155A (11), S. 2771 - 4 (2011)
2.
Zeitschriftenartikel
Kariminejad, A.; Kariminejad, R.; Tzschach, A.; Najafi, H.; Ahmed, A.; Ullmann, R.; Ropers, H.-H.; Kariminejad, M. H.: 11q14.1-11q22.1 deletion in a 1-year-old male with minor dysmorphic features. American Journal of Medical Genetics. Part A. 152A (10), S. 2651 - 2655 (2010)
3.
Zeitschriftenartikel
Tzschach, A.; Bisgaard, A.-M.; Kirchhoff, M.; Graul-Neumann, L. M.; Neitzel, H.; Page, S.; Ahmed, A.; Müller, I.; Erdogan, F.; Ropers, H.-H. et al.; Kalscheuer, V. M.; Ullmann, R.: Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11. European Journal of Human Genetics: EJHG 18 (3), S. 291 - 295 (2010)
4.
Zeitschriftenartikel
Tzschach, A.; Bisgaard, A.-M.; Kirchhoff, M.; Graul-Neumann, L. M.; Neitzel, H.; Page, S.; Ahmed, A.; Müller, I.; Erdogan, F.; Ropers, H.-H. et al.; Kalscheuer, V. M.; Ullmann, R.: Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11. European Journal of Human Genetics: EJHG 18 (3), S. 291 - 295 (2010)
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