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Search Results - Pölsler, L.
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VP25.06: Anophthalmia due to a novel mutation in the SOX2 gene
by
Nanda, M.
,
Gellen, J.
,
Csapo, B.
,
Eisnecker, K.
,
Greimel, P.
,
Duba, H.
,
Pölsler, L.
,
Witsch‐Baumgartner, M.
,
Kampelmuhler, E.
,
Klaritsch, P.
Published in
Ultrasound in obstetrics & gynecology
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P-709 Predictive heatmap in Preimplantation Genetic Testing for Monogenic disorders (PGT-M) and Structural Rearrangements (PGT-SR)
by
Van Der Kelen, A
,
Berckmoes, V
,
Keymolen, K
,
Pölsler, L
,
Cools, W
,
De Vos, A
,
De Vos, M
,
Blockeel, C
,
Fernandez-Gallardo, E
,
De Rycke, M
,
Verdyck, P
,
Hes, F J
,
Verpoest, W
Published in
Human reproduction (Oxford)
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Beidseitiges Neoplasma mammae bei Cowden-Syndrom – ein Fallbericht
by
Edwards, C
,
Czech, T
,
Pölsler, L
,
Brunner, C
,
Egle, D
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Conference Proceeding
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Reorganization of inter‐chromosomal interactions in the 2q37‐deletion syndrome
by
Maass, Philipp G
,
Weise, Anja
,
Rittscher, Katharina
,
Lichtenwald, Julia
,
Barutcu, A Rasim
,
Liehr, Thomas
,
Aydin, Atakan
,
Wefeld‐Neuenfeld, Yvette
,
Pölsler, Laura
,
Tinschert, Sigrid
,
Rinn, John L
,
Luft, Friedrich C
,
Bähring, Sylvia
Published in
The EMBO journal
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