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American Journal of Medical Genetics|May 2, 1997
Deletions of 20p12 in Alagille syndrome: frequency and molecular characterizationI D Krantz, E B Rand, A Genin, et al.
American Journal of Medical Genetics. Part A|June 9, 2005
The adult phenotype in Costello syndromeSusan M White, J M Graham, B Kerr, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 11, 2011
Abnormalities of the upper extremities on fetal magnetic resonance imagingS F Nemec, G Kasprian, P C Brugger, et al.
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.
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