Search Results - Crosby, A. H. 

The natural history of Noonan syndrome: a long‐term follow‐up study by Shaw, A C, Kalidas, K, Crosby, A H, Jeffery, S, Patton, M A

Get full text Get full text Get full text

The Silver Syndrome Variant of Hereditary Spastic Paraplegia Maps to Chromosome 11q12-q14, with Evidence for Genetic Heterogeneity within This Subtype by Patel, H., Hart, P. E., Warner, T. T., Houlston, R. S., Patton, M. A., Jeffery, S., Crosby, A. H.

Get full text Get full text

Genetic mapping of the dentinogenesis imperfecta type II locus. by Crosby, A H, Scherpbier-Heddema, T, Wijmenga, C, Altherr, M R, Murray, J C, Buetow, K H, Dixon, M J

Get full text Get full text

TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies by Klein, C.J., Shi, Y., Fecto, F., Donaghy, M., Nicholson, G., McEntagart, M.E., Crosby, A.H., Wu, Y., Lou, H., McEvoy, K.M., Siddique, T., Deng, H.-X., Dyck, P.J.

Get full text Get full text Get full text

Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development by Simpson, M. A. , Hsu, R. , Keir, L. S. , Hao, J. , Sivapalan, G. , Ernst, L. M. , Zackai, E. H. , Al-Gazali, L. I. , Hulskamp, G. , Kingston, H. M. , Prescott, T. E. , Ion, A. , Patton, M. A. , Murday, V. , George, A. , Crosby, A. H. 

Get full text Get full text