Concepedia

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

Miikka Vikkula, Edwin C.M Madman, Vincent Chi Hang Lui, N.I. Zhidkova, George E. Tiller, Mary B. Goldring, Sylvia E. C. van Beersum, M.C. de Waal Malefijt, F.H.J. van den Hoogen, H.H. Ropers,

Cell · 1995 · 409 citations · 17 references

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References

17

Strategies for multilocus linkage analysis in humans.

G.M. Lathrop, J.-M. Lalouel, Cécile Julier et al. · Proceedings of the National Academy of Sciences · 1984 · 2.6K citations · Full text

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Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

Rita Shiang, Leslie M. Thompson, Yazhen Zhu et al. · Cell · 1994 · 1.3K citations

, , +13

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

William Reardon, Robin M. Winter, Paul Rutland et al. · Nature Genetics · 1994 · 768 citations

, , +6

The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping

Johanna Hästbacka, Albert de la Chapelle, Melanie M. Mahtani et al. · Cell · 1994 · 765 citations

, , +12

A fibrillar collagen gene, Col11a1, is essential for skeletal morphogenesis

Y Li, D.A Lacerda, Matthew L. Warman et al. · Cell · 1995 · 378 citations · Full text

, , +14