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J M Graham

Showing results (341-350 of 360) with videos related to

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American Journal of Medical Genetics|June 1, 1990
Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type IIH J Stern, J M Graham, R S Lachman, et al.
American Journal of Human Genetics|March 31, 2000
Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) geneL B Meira, J M Graham, C R Greenberg, et al.
Clinical Genetics|July 9, 2013
Phenotype-genotype correlations in patients with Marinesco-Sjögren syndromeF Ezgu, P Krejci, S Li, et al.
Genomics|August 11, 1992
Deletion mapping of H-Y antigen to the long arm of the human Y chromosomeM A Cantrell, J S Bogan, E Simpson, et al.
American Journal of Medical Genetics|June 28, 2001
Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3D N Schweitzer, J M Graham, R S Lachman, et al.
European Journal of Clinical Investigation|March 19, 2003
Effects of insulin lispro and chronic vitamin C therapy on postprandial lipaemia, oxidative stress and endothelial function in patients with type 2 diabetes mellitusM Evans, R A Anderson, J C Smith, et al.
Neurology|December 15, 2004
Diffusion tensor imaging for the assessment of upper motor neuron integrity in ALSJ M Graham, N Papadakis, J Evans, et al.
American Journal of Medical Genetics|October 2, 1996
Report from the workshop on Pallister-Hall syndrome and related phenotypesL G Biesecker, M Abbott, J Allen, et al.
Journal of Medical Genetics|January 15, 2003
P63 mutations are not a major cause of non-syndromic split hand/foot malformationX J de Mollerat, D B Everman, C T Morgan, et al.
American Journal of Human Genetics|March 1, 1996
FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicingG A Meyers, D Day, R Goldberg, et al.
Pageof 36

Showing results (341-350 of 360) with videos related to

Sort By:
Pageof 36
American Journal of Medical Genetics|June 1, 1990
Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type IIH J Stern, J M Graham, R S Lachman, et al.
American Journal of Human Genetics|March 31, 2000
Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) geneL B Meira, J M Graham, C R Greenberg, et al.
Clinical Genetics|July 9, 2013
Phenotype-genotype correlations in patients with Marinesco-Sjögren syndromeF Ezgu, P Krejci, S Li, et al.
Genomics|August 11, 1992
Deletion mapping of H-Y antigen to the long arm of the human Y chromosomeM A Cantrell, J S Bogan, E Simpson, et al.
American Journal of Medical Genetics|June 28, 2001
Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3D N Schweitzer, J M Graham, R S Lachman, et al.
European Journal of Clinical Investigation|March 19, 2003
Effects of insulin lispro and chronic vitamin C therapy on postprandial lipaemia, oxidative stress and endothelial function in patients with type 2 diabetes mellitusM Evans, R A Anderson, J C Smith, et al.
Neurology|December 15, 2004
Diffusion tensor imaging for the assessment of upper motor neuron integrity in ALSJ M Graham, N Papadakis, J Evans, et al.
American Journal of Medical Genetics|October 2, 1996
Report from the workshop on Pallister-Hall syndrome and related phenotypesL G Biesecker, M Abbott, J Allen, et al.
Journal of Medical Genetics|January 15, 2003
P63 mutations are not a major cause of non-syndromic split hand/foot malformationX J de Mollerat, D B Everman, C T Morgan, et al.
American Journal of Human Genetics|March 1, 1996
FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicingG A Meyers, D Day, R Goldberg, et al.
Pageof 36