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Clinical Genetics|February 6, 2013
Clinical and genetic heterogeneity of amyotrophic lateral sclerosisM Sabatelli, A Conte, M ZollinoClinical Genetics|February 13, 2013
Geographical distribution of Slovenian BRCA1/2 families according to family origin: implications for genetic screeningM Krajc, V Zadnik, S Novaković, et al.Clinical Genetics|September 5, 2013
Risk of having BRCA1 mutation in high-risk women with triple-negative breast cancer: a meta-analysisN M Tun, G Villani, K Ong, et al.Clinical Genetics|September 5, 2013
Implementation of high-resolution SNP arrays in the investigation of fetuses with ultrasound malformations: 5 years of clinical experienceC Liao, F Fu, R Li, et al.Clinical Genetics|September 5, 2013
National mutation study among Danish patients with hereditary haemorrhagic telangiectasiaP M Tørring, K Brusgaard, L B Ousager, et al.Clinical Genetics|July 22, 2014
Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelinesJ A Anderson, R Z Hayeems, C Shuman, et al.Clinical Genetics|July 23, 2014
Carrier screening of RTEL1 mutations in the Ashkenazi Jewish populationA M Fedick, L Shi, C Jalas, et al.Clinical Genetics|August 1, 2014
Autosomal dominant IFIH1 gain-of-function mutations cause Aicardi-Goutières syndromeJ DiamondClinical Genetics|August 5, 2014
Molecular and computational analyses of genes involved in mannose 6-phosphate independent traffickingM F Coutinho, L Lacerda, E Pinto, et al.Clinical Genetics|September 1, 1986
Increased levels of apo-transcobalamins I and II in amniotic fluid from pregnant women with previous neural tube defect offspringP Magnus, E M Magnus, K BergPageof 718