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The Journal of Pediatrics|July 1, 1992
Dextromethorphan and high-dose benzoate therapy for nonketotic hyperglycinemia in an infantA Hamosh, J W McDonald, D Valle, et al.American Journal of Human Genetics|March 3, 1999
A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 geneP L Tavormina, G A Bellus, M K Webster, et al.Development (Cambridge, England)|May 1, 1990
The Xenopus XIHbox 6 homeo protein, a marker of posterior neural induction, is expressed in proliferating neuronsC V Wright, E A Morita, D J Wilkin, et al.Human Mutation|October 23, 2001
Twenty-two novel LMX1B mutations identified in nail patella syndrome (NPS) patientsJ D Hamlington, C Jones, I McIntoshOsteoarthritis and Cartilage|January 18, 2006
Comparison of gene expression profile between human chondrons and chondrocytes: a cDNA microarray studyZ Zhang, J Fan, K G Becker, et al.The Journal of Pediatrics|May 15, 1998
Sleep-disordered breathing in children with achondroplasiaP J Mogayzel, J L Carroll, G M Loughlin, et al.Cell Structure and Function|July 8, 2000
The pleiotropic effects of fibroblast growth factor receptors in mammalian developmentI McIntosh, G A Bellus, E W JabHuman Mutation|November 26, 1999
Restricted distribution of loss-of-function mutations within the LMX1B genes of nail-patella syndrome patientsM V Clough, J D Hamlington, I McIntoshJournal of Medical Genetics|May 1, 1991
The incidence of different cystic fibrosis mutations in the Scottish population: effects on prenatal diagnosis and genetic counsellingA E Shrimpton, I McIntosh, D J BrockMolecular and Cellular Probes|August 1, 1992
Detection of Pseudomonas aeruginosa in sputum from cystic fibrosis patients by the polymerase chain reactionI McIntosh, J R Govan, D J BrockPageof 17