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Clinical Genetics|March 5, 1999
Lower extremity counterpart of the Poland syndromeM Silengo, M Lerone, M Seri, et al.
Clinical Genetics|March 5, 1999
Kenny-Caffey syndrome: an Arab variant?M A Sabry, T I Farag, A A Shaltout, et al.
Clinical Genetics|March 5, 1999
Missense mutations in phosphomannomutase 2 gene in two Japanese families with carbohydrate-deficient glycoprotein syndrome type 1I Kondo, K Mizugishi, Y Yoneda, et al.
Clinical Genetics|March 5, 1999
X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisationH Woffendin, T Jakins, M Jouet, et al.
Clinical Genetics|February 3, 2006
Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genesP Verdyck, B Blaumeiser, M Holder-Espinasse, et al.
Clinical Genetics|January 26, 2006
Prevalence of HFE C282Y and H63D in Jewish populations and clinical implications of H63D homozygosityM Matas, P Guix, J A Castro, et al.
Clinical Genetics|January 26, 2006
Educational outcomes of a workplace screening program for genetic susceptibility to hemochromatosisA E Nisselle, V R Collins, A A Gason, et al.
Clinical Genetics|March 18, 2006
Genetic knowledge and moral responsibility: ambiguity at the interface of genetic research and clinical practiceD Pullman, K Hodgkinson
Clinical Genetics|March 18, 2006
Comparative transcriptome maps: a new approach to the diagnosis of colorectal carcinoma patients using cDNA microarraysE Jansová, I Koutná, P Krontorád, et al.
Clinical Genetics|March 18, 2006
Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutationsL-E Wehner, B J Folz, L Argyriou, et al.
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