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C M Hall

Showing results (181-190 of 188) with videos related to

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European Journal of Pediatrics|December 14, 1999
Sacral dysgenesis associated with terminal deletion of chromosome 7q: a report of two familiesJ Wang, L Spitz, R Hayward, et al.
Clinical Endocrinology|February 20, 2009
Likelihood of persistent GH deficiency into late adolescence: relationship to the presence of an ectopic or normally sited posterior pituitary glandP G Murray, C Hague, O Fafoula, et al.
Journal of Periodontal Research|November 1, 1987
Effects of flurbiprofen on the progression of periodontitis in Macaca mulattaS Offenbacher, L D Braswell, A S Loos, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locusL J Pulleyn, W Reardon, D Wilkes, et al.
Journal of Lipid Research|July 1, 1995
Kinetic evidence for both a fast and a slow secretory pathway for apolipoprotein A-I in humansW R Fisher, V Venkatakrishnan, L A Zech, et al.
Journal of Medical Genetics|September 3, 2008
Skewed X inactivation is associated with phenotype in a female with adrenal hypoplasia congenitaM G Shaikh, L Boyes, H Kingston, et al.
European Journal of Endocrinology|August 29, 2003
IGF-I and IGF-binding protein-3 measurements on filter paper blood spots in children and adolescents on GH treatment: use in monitoring and as markers of growth performanceU Das, A J Whatmore, J Khosravi, et al.
Journal of Medical Genetics|August 1, 1997
Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosisW Reardon, D Wilkes, P Rutland, et al.
Pageof 19

Showing results (181-190 of 188) with videos related to

Sort By:
Pageof 19
You have reached the last page of results.This site can display upto 188 results.
European Journal of Pediatrics|December 14, 1999
Sacral dysgenesis associated with terminal deletion of chromosome 7q: a report of two familiesJ Wang, L Spitz, R Hayward, et al.
Clinical Endocrinology|February 20, 2009
Likelihood of persistent GH deficiency into late adolescence: relationship to the presence of an ectopic or normally sited posterior pituitary glandP G Murray, C Hague, O Fafoula, et al.
Journal of Periodontal Research|November 1, 1987
Effects of flurbiprofen on the progression of periodontitis in Macaca mulattaS Offenbacher, L D Braswell, A S Loos, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locusL J Pulleyn, W Reardon, D Wilkes, et al.
Journal of Lipid Research|July 1, 1995
Kinetic evidence for both a fast and a slow secretory pathway for apolipoprotein A-I in humansW R Fisher, V Venkatakrishnan, L A Zech, et al.
Journal of Medical Genetics|September 3, 2008
Skewed X inactivation is associated with phenotype in a female with adrenal hypoplasia congenitaM G Shaikh, L Boyes, H Kingston, et al.
European Journal of Endocrinology|August 29, 2003
IGF-I and IGF-binding protein-3 measurements on filter paper blood spots in children and adolescents on GH treatment: use in monitoring and as markers of growth performanceU Das, A J Whatmore, J Khosravi, et al.
Journal of Medical Genetics|August 1, 1997
Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosisW Reardon, D Wilkes, P Rutland, et al.
Pageof 19