Search Results - "Kittner, G"

Evidence for a new microdeletion syndrome in 15q21 by Liehr, T, Starke, H, Heller, A, Weise, A, Beensen, V, Senger, G, Kittner, G, Prechtel, M, Claussen, U, Seidel, J

“…We report on the fourth known case with an interstitial deletion in 15q21. In the present case the breakpoints have been determined by GTG-banding,…”
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Conspicuous GTG-banding results of the centromere-near region can be caused by alphoid DNA heteromorphism by Liehr, T., Ziegler, M., Starke, H., Heller, A., Kuechler, A., Kittner, G., Beensen, V., Seidel, J., Häßler, H., Müsebeck, J., Claussen, U.

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First case of trisomy 13 plus mosaic trisomy 1q by Liehr, Thomas, Schmidt, Matthias, Starke, Heike, Ziegler, Monika, Kittner, Gabriele, Heller, Anita, Rubtsov, Nikolai, Trifonov, Vladimir, Claussen, Uwe

“…In a case with severe sonographic abnormalities followed by missed abortion in week 14 + 5 days, cytogenetic analysis was performed on placental tissue. A…”
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