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Clinical Genetics|December 1, 1990
Diagnosis of familial amyloidotic polyneuropathy in FranceF Satier, W C Nichols, M D BensonClinical Genetics|April 2, 2014
Olfaction evaluation and correlation with brain atrophy in Bardet-Biedl syndromeJ-J Braun, V Noblet, M Durand, et al.Clinical Genetics|April 5, 2014
De novo EEF1A2 mutations in patients with characteristic facial features, intellectual disability, autistic behaviors and epilepsyJ Nakajima, N Okamoto, J Tohyama, et al.Clinical Genetics|March 20, 2014
Pharmacogenetics of beta2 adrenergic receptor agonists in asthma managementV E OrtegaClinical Genetics|July 1, 1985
Genetic regulation of the kinetics of glucose-induced insulin release in man. Studies in families with diabetic and non-diabetic probandsL Iselius, J Lindsten, N E Morton, et al.Clinical Genetics|May 22, 2008
Investigating genetic discrimination in Australia: a large-scale survey of clinical genetics clientsS Taylor, S Treloar, K Barlow-Stewart, et al.Clinical Genetics|April 12, 2014
Antisense-mediated therapeutic pseudoexon skipping in TMEM165-CDGP Yuste-Checa, C Medrano, A Gámez, et al.Clinical Genetics|April 15, 2014
Hypertrophic pyloric stenosis in twins; genetic or environmental factorsH Ö Gezer, P Oguzkurt, A Temiz, et al.Clinical Genetics|April 26, 2008
Severe mandibuloacral dysplasia caused by novel compound heterozygous ZMPSTE24 mutations in two Japanese siblingsY Miyoshi, M Akagi, A K Agarwal, et al.Clinical Genetics|May 13, 2014
Determination of the allelic frequency in Smith-Lemli-Opitz syndrome by analysis of massively parallel sequencing data setsJ L Cross, J Iben, C L Simpson, et al.Pageof 719