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Clinical Genetics|September 25, 2008
Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2B C Ballif, A Theisen, D M McDonald-McGinn, et al.Clinical Genetics|September 12, 2008
Promoting ectopic pancreatic fates: pancreas development and future diabetes therapiesE J Pearl, M E HorbClinical Genetics|September 12, 2008
Confirmation of RAX gene involvement in human anophthalmiaL Lequeux, M Rio, A Vigouroux, et al.Clinical Genetics|February 1, 1990
Prenatal diagnosis in Pelizaeus-Merzbacher disease using RFLP analysisJ Mäenpää, E Lindahl, P Aula, et al.Clinical Genetics|March 1, 1990
Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial resultsH Kääriäinen, M Lindlöf, H Somer, et al.Clinical Genetics|January 1, 1990
Diagnostic molecular genetics of the fragile XG R Sutherland, J C MulleyClinical Genetics|May 1, 1991
Cutis laxa: autosomal dominant inheritance in five generationsA Damkier, F Brandrup, H StarklintClinical Genetics|February 14, 2009
Cystic kidney diseases and planar cell polarity signalingR L Bacallao, H McNeillClinical Genetics|February 14, 2009
Comparison of proactive and usual approaches to offering predictive testing for BRCA1/2 mutations in unaffected relativesD G R Evans, A Binchy, A Shenton, et al.Clinical Genetics|March 27, 2009
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sampleM L Mostacciuolo, E Pastorello, G Vazza, et al.Pageof 718