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A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis. [electronic resource] by
- Trappe, R
- Böhm, D
- Kohlhase, J
- Weise, A
- Liehr, T
- Essers, G
- Meins, M
- Zoll, B
- Bartels, I
- Burfeind, P
Producer: 20030404
In:
Cytogenetic and genome research vol. 98
Availability: No items available.
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18.
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Partial trisomy of chromosome 22 resulting from an interstitial duplication of 22q11.2 in a child with typical cat eye syndrome. [electronic resource] by
- Meins, M
- Burfeind, P
- Motsch, S
- Trappe, R
- Bartmus, D
- Langer, S
- Speicher, M R
- Mühlendyck, H
- Bartels, I
- Zoll, B
Producer: 20030805
In:
Journal of medical genetics vol. 40
Availability: No items available.
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19.
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Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander disease. [electronic resource] by
- Hartmann, H
- Herchenbach, J
- Stephani, U
- Ledaal, P
- Donnerstag, F
- Lücke, T
- Das, A M
- Christen, H J
- Hagedorn, M
- Meins, M
Producer: 20080214
In:
Neuropediatrics vol. 38
Availability: No items available.
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Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa. [electronic resource] by
- Grüning, G
- Millan, J M
- Meins, M
- Beneyto, M
- Caballero, M
- Apfelstedt-Sylla, E
- Bosch, R
- Zrenner, E
- Prieto, F
- Gal, A
Producer: 19940804
In:
Human mutation vol. 3
Availability: No items available.
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