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Journal of Craniofacial Genetics and Developmental Biology|July 1, 1991
Clouston syndrome: a rare autosomal dominant trait with palmoplantar hyperkeratosis and alopeciaR R Patel, D Bixler, A L NorinsNature Reviews. Endocrinology|April 5, 2012
The changing epidemiology of iodine deficiencyMu Li, Creswell J EastmanBest Practice & Research. Clinical Endocrinology & Metabolism|February 23, 2010
Neonatal TSH screening: is it a sensitive and reliable tool for monitoring iodine status in populations?Mu Li, Creswell J EastmanClinical Genetics|May 1, 1985
Gustatory lacrimation in association with the branchio-oto-renal syndromeJ W Preisch, D Bixler, F D EllisJournal of Craniofacial Genetics and Developmental Biology|January 1, 1983
Stickler syndrome: a cephalometric study of the faceS S Saksena, D Bixler, P I YuJournal of Craniofacial Genetics and Developmental Biology|January 1, 1985
Velopharyngeal variations in relatives of cleft-affected individualsJ P Huston, D Bixler, P I YuJournal of Craniofacial Genetics and Developmental Biology|January 1, 1985
Genetic analysis in families with van der Woude syndromeA B Burdick, D Bixler, C L PuckettNestle Nutrition Institute Workshop Series|April 1, 2015
Current challenges in meeting global iodine requirementsCreswell J Eastman, Pieter JoosteThe Medical Journal of Australia|December 21, 2002
Working with funding agencies in the delivery of healthcare in the Asia Pacific regionMu Li, Creswell J EastmanThe Australian Journal of Experimental Biology and Medical Science|August 1, 1981
The erythrocyte insulin receptorA McElduff, C J EastmanPageof 27