Showing results (221-230 of 335) with videos related to

Sort By:
Pageof 34
AJNR. American Journal of Neuroradiology|September 1, 1996
Imaging findings of the developing temporal bone in fetal specimensW R Nemzek, H A Brodie, B W Chong, et al.
American Journal of Medical Genetics. Part A|January 19, 2010
Survival of Texas infants born with trisomies 21, 18, and 13Catherine Vendola, Mark Canfield, Stephen P Daiger, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|July 27, 2001
Calreticulin, PDI, Grp94 and BiP chaperone proteins are associated with retained COMP in pseudoachondroplasia chondrocytesJ T Hecht, E Hayes, M Snuggs, et al.
International Journal of Molecular Sciences|January 11, 2025
Loss of CHOP Prevents Joint Degeneration and Pain in a Mouse Model of PseudoachondroplasiaJacqueline T Hecht, Alka C Veerisetty, Mohammad G Hossain, et al.
Genomics|December 1, 1993
Linkage of typical pseudoachondroplasia to chromosome 19J T Hecht, C A Francomano, M D Briggs, et al.
Blood|October 1, 1981
Histochemical demonstration of terminal deoxynucleotidyl transferase in leukemiaT Hecht, S J Forman, U S Winkler, et al.
Nature Genetics|September 1, 1993
A type X collagen mutation causes Schmid metaphyseal chondrodysplasiaM L Warman, M Abbott, S S Apte, et al.
American Journal of Human Genetics|April 1, 1992
Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypesG A Greenhaw, A Hebert, M E Duke-Woodside, et al.
European Journal of Human Genetics : EJHG|July 3, 2014
Mutations in COL27A1 cause Steel syndrome and suggest a founder mutation effect in the Puerto Rican populationClaudia Gonzaga-Jauregui, Candace N Gamble, Bo Yuan, et al.
Pageof 34