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P S Hart

Showing results (41-50 of 52) with videos related to

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Journal of Medical Genetics|February 9, 2000
Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutationT C Hart, P S Hart, M D Michalec, et al.
Journal of Medical Genetics|March 19, 2002
A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotypeJ Tarleton, A Kenneson, A K Taylor, et al.
Connective Tissue Research|September 4, 2003
Relationship of phenotype and genotype in X-linked amelogenesis imperfectaJ T Wright, P S Hart, M J Aldred, et al.
The Journal of Pediatrics|January 1, 1990
Partial biotinidase deficiency: clinical and biochemical featuresJ R McVoy, H L Levy, M Lawler, et al.
Developmental Biology|November 11, 2008
In vivo impact of a 4 bp deletion mutation in the DLX3 gene on bone developmentS J Choi, G D Roodman, J Q Feng, et al.
Journal of Medical Genetics|December 20, 2003
Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defectsT C Hart, P S Hart, M C Gorry, et al.
Journal of Medical Genetics|February 7, 2001
Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefèvre syndrome patientsY Zhang, T Lundgren, S Renvert, et al.
Genes and Immunity|February 22, 2003
Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patientsY Zhang, R Syed, C Uygar, et al.
Journal of Medical Genetics|December 10, 2002
Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathyT C Hart, M C Gorry, P S Hart, et al.
Journal of Medical Genetics|February 9, 2000
Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin CT C Hart, P S Hart, M D Michalec, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|February 9, 2000
Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutationT C Hart, P S Hart, M D Michalec, et al.
Journal of Medical Genetics|March 19, 2002
A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotypeJ Tarleton, A Kenneson, A K Taylor, et al.
Connective Tissue Research|September 4, 2003
Relationship of phenotype and genotype in X-linked amelogenesis imperfectaJ T Wright, P S Hart, M J Aldred, et al.
The Journal of Pediatrics|January 1, 1990
Partial biotinidase deficiency: clinical and biochemical featuresJ R McVoy, H L Levy, M Lawler, et al.
Developmental Biology|November 11, 2008
In vivo impact of a 4 bp deletion mutation in the DLX3 gene on bone developmentS J Choi, G D Roodman, J Q Feng, et al.
Journal of Medical Genetics|December 20, 2003
Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defectsT C Hart, P S Hart, M C Gorry, et al.
Journal of Medical Genetics|February 7, 2001
Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefèvre syndrome patientsY Zhang, T Lundgren, S Renvert, et al.
Genes and Immunity|February 22, 2003
Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patientsY Zhang, R Syed, C Uygar, et al.
Journal of Medical Genetics|December 10, 2002
Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathyT C Hart, M C Gorry, P S Hart, et al.
Journal of Medical Genetics|February 9, 2000
Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin CT C Hart, P S Hart, M D Michalec, et al.
Pageof 6