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Clinical Genetics|February 27, 2013
Modes of delivery of genetic testing services and the uptake of cancer risk management strategies in BRCA1 and BRCA2 carriersT Pal, J-H Lee, A Besharat, et al.
Clinical Genetics|May 14, 2013
Genetics of the corneal endothelial dystrophies: an evidence-based reviewA J Aldave, J Han, R F Frausto
Clinical Genetics|May 14, 2013
eyeGENE®: a vision community resource facilitating patient care and paving the path for research through molecular diagnostic testingD Blain, K E Goetz, R Ayyagari, et al.
Clinical Genetics|April 30, 2013
The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findingsF C Connell, K Gordon, G Brice, et al.
Clinical Genetics|January 29, 2013
The uptake and outcome of prenatal and pre-implantation genetic diagnosis for Huntington's disease in the Netherlands (1998-2008)M C van Rij, P A M de Koning Gans, M J van Belzen, et al.
Clinical Genetics|August 1, 1989
Catalase and glutathione peroxidase activity in cells with trisomy 21N Crosti, J Bajer, M Gentile, et al.
Clinical Genetics|October 8, 2014
Consanguinity and founder effect for Gaucher disease mutation G377S in a population from Tabuleiro do Norte, Northeastern BrazilR G Chaves, L da Veiga Pereira, F T de Araújo, et al.
Clinical Genetics|November 1, 1989
Fabry's diseaseL Hasholt, A Wandall, S A Sørensen
Clinical Genetics|September 9, 2014
BRCA1 and BRCA2 mutations and the risk for colorectal cancerV Sopik, C Phelan, C Cybulski, et al.
Clinical Genetics|August 19, 2014
Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorderA Chaudhry, A Noor, B Degagne, et al.
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