D L Rimoin|J M Graham - JoVE Visualize

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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 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.

Clinical Radiology|May 19, 1998

Radiological malformations of the ear in Pendred syndromeP D Phelps, R A Coffey, R C Trembath, et al.

American Journal of Medical Genetics|December 31, 1997

Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical GeneticsC J Curry, R E Stevenson, D Aughton, et al.

Journal of Medical Genetics|September 23, 2008

Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndromeM J Lyons, J M Graham, G Neri, et al.

Human Molecular Genetics|January 15, 1999

The spectrum of mutations in UBE3A causing Angelman syndromeP Fang, E Lev-Lehman, T F Tsai, et al.

Clinical Genetics|August 2, 2011

Ehlers-Danlos arthrochalasia type (VIIA-B)--expanding the phenotype: from prenatal life through adulthoodM Klaassens, E Reinstein, Y Hilhorst-Hofstee, et al.

Human Genetics|November 10, 2001

Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformationsM J Rosenberg, C Killoran, L Dziadzio, et al.

Pageof 42

Showing results (401-410 of 412) with videos related to

Sort By:

Pageof 42

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 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.

Clinical Radiology|May 19, 1998

Radiological malformations of the ear in Pendred syndromeP D Phelps, R A Coffey, R C Trembath, et al.

American Journal of Medical Genetics|December 31, 1997

Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical GeneticsC J Curry, R E Stevenson, D Aughton, et al.

Journal of Medical Genetics|September 23, 2008

Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndromeM J Lyons, J M Graham, G Neri, et al.

Human Molecular Genetics|January 15, 1999

The spectrum of mutations in UBE3A causing Angelman syndromeP Fang, E Lev-Lehman, T F Tsai, et al.

Clinical Genetics|August 2, 2011

Ehlers-Danlos arthrochalasia type (VIIA-B)--expanding the phenotype: from prenatal life through adulthoodM Klaassens, E Reinstein, Y Hilhorst-Hofstee, et al.

Human Genetics|November 10, 2001

Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformationsM J Rosenberg, C Killoran, L Dziadzio, et al.

Pageof 42