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P S Hart

Showing results (21-30 of 52) with videos related to

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Molecular Genetics and Metabolism|June 27, 2002
Identification of a novel cathepsin C mutation (p.W185X) in a Brazilian kindred with Papillon-Lefèvre syndromeP S Hart, D Pallos, Y Zhang, et al.
Prenatal Diagnosis|March 12, 1999
Prenatal interphase detection by FISH of a sex chromosome mosaicism when cytogenetics reports a pseudomosaicismM J Pettenati, M N Berry, P S Hart, et al.
Neurology|March 19, 2008
Uniparental disomy of chromosome 1 causing concurrent Charcot-Marie-Tooth and Gaucher disease Type 3W S Benko, K S Hruska, N Nagan, et al.
Archives of Oral Biology|April 2, 2002
Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutationsP S Hart, M J Aldred, P J M Crawford, et al.
Prenatal Diagnosis|March 1, 1990
Prenatal detection of non-cardiac rhabdomyosarcomaP S Hart, J Bodurtha, F O Redwine, et al.
Journal of Dental Research|September 27, 2000
Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutationD B Ravassipour, P S Hart, T C Hart, et al.
Journal of Medical Genetics|July 6, 2004
Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfectaP S Hart, T C Hart, M D Michalec, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 21, 2000
An integrated physical and genetic map of the PLS locus interval on chromosome 11q14T C Hart, S J Walker, D W Bowden, et al.
Medical and Pediatric Oncology|June 8, 1999
Hereditary persistence of alpha-fetoprotein in a child with testicular germ cell tumorP K Cochran, A R Chauvenet, P S Hart, et al.
Anesthesiology|May 1, 1994
Rapid increase in desflurane concentration is associated with greater transient cardiovascular stimulation than with rapid increase in isoflurane concentration in humansR B Weiskopf, M A Moore, E I Eger, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
Molecular Genetics and Metabolism|June 27, 2002
Identification of a novel cathepsin C mutation (p.W185X) in a Brazilian kindred with Papillon-Lefèvre syndromeP S Hart, D Pallos, Y Zhang, et al.
Prenatal Diagnosis|March 12, 1999
Prenatal interphase detection by FISH of a sex chromosome mosaicism when cytogenetics reports a pseudomosaicismM J Pettenati, M N Berry, P S Hart, et al.
Neurology|March 19, 2008
Uniparental disomy of chromosome 1 causing concurrent Charcot-Marie-Tooth and Gaucher disease Type 3W S Benko, K S Hruska, N Nagan, et al.
Archives of Oral Biology|April 2, 2002
Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutationsP S Hart, M J Aldred, P J M Crawford, et al.
Prenatal Diagnosis|March 1, 1990
Prenatal detection of non-cardiac rhabdomyosarcomaP S Hart, J Bodurtha, F O Redwine, et al.
Journal of Dental Research|September 27, 2000
Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutationD B Ravassipour, P S Hart, T C Hart, et al.
Journal of Medical Genetics|July 6, 2004
Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfectaP S Hart, T C Hart, M D Michalec, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 21, 2000
An integrated physical and genetic map of the PLS locus interval on chromosome 11q14T C Hart, S J Walker, D W Bowden, et al.
Medical and Pediatric Oncology|June 8, 1999
Hereditary persistence of alpha-fetoprotein in a child with testicular germ cell tumorP K Cochran, A R Chauvenet, P S Hart, et al.
Anesthesiology|May 1, 1994
Rapid increase in desflurane concentration is associated with greater transient cardiovascular stimulation than with rapid increase in isoflurane concentration in humansR B Weiskopf, M A Moore, E I Eger, et al.
Pageof 6