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Clinical Genetics|April 8, 2010
Safety and cardiovascular behavior during pulmonary function in patients with Marfan syndromeG F B Cipriano, P A T Peres, G Cipriano, et al.Clinical Genetics|September 14, 2007
Molecular analysis and long-term clinical evaluation of three siblings with Alström syndromeR K Ozgül, I Satman, G B Collin, et al.Clinical Genetics|September 14, 2007
Auditory pathology in cri-du-chat (5p-) syndrome: phenotypic evidence for auditory neuropathyD SwanepoelClinical Genetics|October 10, 2006
Presymptomatic and predictive genetic testing in minors: a systematic review of guidelines and position papersP Borry, L Stultiens, H Nys, et al.Clinical Genetics|October 10, 2006
Maturity of judgement in decision making for predictive testing for nontreatable adult-onset neurogenetic conditions: a case against predictive testing of minorsF H RichardsClinical Genetics|September 18, 2007
TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai populationK Suphapeetiporn, S Tongkobpetch, P Siriwan, et al.Clinical Genetics|May 8, 2009
Plumbing in the embryo: developmental defects of the urinary tractsN Uetani, M BouchardClinical Genetics|May 29, 2009
Recurrence risk due to germ line mosaicism: Duchenne and Becker muscular dystrophyA T J M Helderman-van den Enden, R de Jong, J T den Dunnen, et al.Clinical Genetics|May 29, 2009
Proven germline mosaicism in a father of two children with CHARGE syndromeS Pauli, L Pieper, J Häberle, et al.Clinical Genetics|June 23, 2009
Multiplex ligation-dependent probe amplification analysis to screen for deletions and duplications of the LDLR gene in patients with familial hypercholesterolaemiaA Taylor, B Martin, D Wang, et al.Pageof 718