Osteochondrodysplasias
This graph shows the total number of publications written about "Osteochondrodysplasias" by people in the URMC Research Network by year, and whether "Osteochondrodysplasias" was a major or minor topic of these publication.
Below are the most recent publications written about "Osteochondrodysplasias" by people in Profiles.
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Morello R, Bertin TK, Chen Y, Hicks J, Tonachini L, Monticone M, Castagnola P, Rauch F, Glorieux FH, Vranka J, Bächinger HP, Pace JM, Schwarze U, Byers PH, Weis M, Fernandes RJ, Eyre DR, Yao Z, Boyce BF, Lee B. CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta. Cell. 2006 Oct 20; 127(2):291-304.
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Hilton MJ, Sawyer JM, Gutiérrez L, Hogart A, Kung TC, Wells DE. Analysis of novel and recurrent mutations responsible for the tricho-rhino-phalangeal syndromes. J Hum Genet. 2002; 47(3):103-6.
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Calvi LM, Schipani E. The PTH/PTHrP receptor in Jansen's metaphyseal chondrodysplasia. J Endocrinol Invest. 2000 Sep; 23(8):545-54.
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