Chromosomal Variants in Klinefelter Syndrome von Frühmesser, A., Kotzot, D.

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Modification of risk for cancer as a coincidental finding in DNA array investigation von Rostasy, K, Fauth, C, Gautsch, K, Laimer, I, Krabichler, B, Wimmer, K, Frühmesser, A, Kotzot, D, Moshir, S

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Parental Origin of de novo Cytogenetically Balanced Reciprocal Non-Robertsonian Translocations von Höckner, M., Spreiz, A., Frühmesser, A., Tzschach, A., Dufke, A., Rittinger, O., Kalscheuer, V., Singer, S., Erdel, M., Fauth, C., Grossmann, V., Utermann, G., Zschocke, J., Kotzot, D.

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Supplementary Material for: Chromosomal Variants in Klinefelter Syndrome von Frühmesser, A., Kotzot, D.

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Single nucleotide polymorphism array analysis in men with idiopathic azoospermia or oligoasthenozoospermia syndrome von Frühmesser, Anne, Ph.D, Vogt, Peter H., Ph.D, Zimmer, Jutta, Witsch-Baumgartner, Martina, Ph.D, Fauth, Christine, M.D, Zschocke, Johannes, Ph.D., M.D, Pinggera, Germar-Michael, M.D, Kotzot, Dieter, M.D

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Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation von Frühmesser, Anne, Blake, Jonathon, Haberlandt, Edda, Baying, Bianka, Raeder, Benjamin, Runz, Heiko, Spreiz, Ana, Fauth, Christine, Benes, Vladimir, Utermann, Gerd, Zschocke, Johannes, Kotzot, Dieter

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Effects of deletion and duplication in a patient with a 46,XX,der(7)t(7;17)(q36;p13)mat karyotype von Frühmesser, Anne, Haberlandt, Edda, Judmaier, Werner, Schinzel, Albert, Utermann, Barbara, Erdel, Martin, Fauth, Christine, Utermann, Gerd, Zschocke, Johannes, Kotzot, Dieter

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Severe growth retardation, delayed bone age, and facial dysmorphism in two patients with microduplications in 2p16 → p22 von Blassnig-Ezeh, Anya, Bandelier, Claude, Frühmesser, Anne, Revencu, Nicole, Krabichler, Birgit, Beauloye, Véronique, Ravoet, Marie, Fauth, Christine, Zschocke, Johannes, Simma, Burkhard, Kotzot, Dieter

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Combined Dup(7)(q22.1q32.2), Inv(7)(q31.31q31.33), and Ins(7;19)(q22.1;p13.2p13.2) in a 12-year-old boy with developmental delay and various dysmorphism von Frühmesser, Anne, Erdel, Martin, Duba, Hans-Christoph, Fauth, Christine, Amberger, Albert, Utermann, Gerd, Zschocke, Johannes, Kotzot, Dieter

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Effects of deletion and duplication in a patient with a 46,XX,der(7)t(7;17)(q36;p13)mat karyotype von Frühmesser, Anne, Haberlandt, Edda, Judmaier, Werner, Schinzel, Albert, Utermann, Barbara, Erdel, Martin, Fauth, Christine, Utermann, Gerd, Zschocke, Johannes, Kotzot, Dieter

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Effects of deletion and duplication in a patient with a 46,XX,der(7)t(7;17)(q36;p13)mat karyotype von Frühmesser, Anne, Haberlandt, Edda, Judmaier, Werner, Schinzel, Albert, Utermann, Barbara, Erdel, Martin, Fauth, Christine, Utermann, Gerd, Zschocke, Johannes, Kotzot, Dieter

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