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Archives of Disease in Childhood|August 2, 2006
Reference chart for relative weight change to detect hypernatraemic dehydrationPaula van Dommelen, Jacobus P van Wouwe, Jacqueline M Breuning-Boers, et al.Human Genetics|July 1, 1995
Autosomal dominant polycystic kidney disease: evidence for the existence of a third locus in a Portuguese familyS de Almeida, E de Almeida, D Peters, et al.European Journal of Human Genetics : EJHG|April 21, 2001
A Rett syndrome patient with a ring X chromosome: further evidence for skewing of X inactivation and heterogeneity in the aetiology of the diseaseC Rosenberg, C H Wouters, K Szuhai, et al.American Journal of Medical Genetics|January 23, 2002
Using a roster and haplotyping is useful in risk assessment for persons with intermediate and reduced penetrance alleles in Huntington diseaseA Maat-Kievit, P Helderman-van den Enden, M Losekoot, et al.Lancet (London, England)|February 19, 1999
Comparison of phenotypes of polycystic kidney disease types 1 and 2. European PKD1-PKD2 Study GroupN Hateboer, M A v Dijk, N Bogdanova, et al.Genomics|August 1, 1992
Evaluation of a cosmid contig physical map of human chromosome 16R L Stallings, N A Doggett, D Callen, et al.Nature Genetics|June 3, 2000
Mutations in ABCC6 cause pseudoxanthoma elasticumA A Bergen, A S Plomp, E J Schuurman, et al.Genomics|December 10, 1999
Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16O Le Saux, Z Urban, H H Göring, et al.Chest|May 7, 2026
Comparison of Hemodynamic Responses to Balloon Pulmonary Angioplasty in Chronic Thromboembolic Pulmonary Hypertension in Japan and the Netherlands: a multicenter studySatoshi Higuchi, Konstantinos Mantzios, Takatoyo Kiko, et al.Pageof 2