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A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients. [electronic resource] by
- Rall, Katharina
- Barresi, Gianmaria
- Walter, Michael
- Poths, Sven
- Haebig, Karina
- Schaeferhoff, Karin
- Schoenfisch, Birgitt
- Riess, Olaf
- Wallwiener, Diethelm
- Bonin, Michael
- Brucker, Sara
Producer: 20111018
In:
Orphanet journal of rare diseases vol. 6
Availability: No items available.
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Structural and functional phenotyping in the cone-specific photoreceptor function loss 1 (cpfl1) mouse mutant - a model of cone dystrophies. [electronic resource] by
- Fischer, M Dominik
- Tanimoto, Naoyuki
- Beck, Susanne C
- Huber, Gesine
- Schaeferhoff, Karin
- Michalakis, Stylianos
- Riess, Olaf
- Wissinger, Bernd
- Biel, Martin
- Bonin, Michael
- Seeliger, Mathias W
Producer: 20110912
In:
Advances in experimental medicine and biology vol. 664
Availability: No items available.
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In vivo analysis of cone survival in mice. [electronic resource] by
- Beck, Susanne C
- Schaeferhoff, Karin
- Michalakis, Stylianos
- Fischer, M Dominik
- Huber, Gesine
- Rieger, Norman
- Riess, Olaf
- Wissinger, Bernd
- Biel, Martin
- Bonin, Michael
- Seeliger, Mathias W
- Tanimoto, Naoyuki
Producer: 20100203
In:
Investigative ophthalmology & visual science vol. 51
Availability: No items available.
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