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Characterization of SHOX deletions in Leri-Weill dyschondrosteosis (LWD) reveals genetic heterogeneity and no recombination hotspots. [electronic resource] by
- Benito-Sanz, Sara
- Gorbenko del Blanco, Darya
- Huber, Celine
- Thomas, N Simon
- Aza-Carmona, Miriam
- Bunyan, David
- Maloney, Vivienne
- Argente, Jesús
- Cormier-Daire, Valérie
- Campos-Barros, Angel
- Heath, Karen E
Producer: 20060914
In:
American journal of human genetics vol. 79
Availability: No items available.
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