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Das B ; Goyal MK ; Bhatkar SR ; Vinny PW ; Modi M ; Lal V ; Gayathri N ; Mahadevan A ; Radotra BD | 2016Article
Udhayabanu T, Author ; Subramanian VS ; Teafatiller T ; Gowda VK ; Raghavan VS ; Varalakshmi P ; Said HM ; Ashokkumar B | 2016Article
Landfeldt E, Author | 2016Comment on: The prevalence of neuromuscular disease in the paediatric population in Yorkshire, UK; variation by ethnicity and deprivation status. [Dev Med Child Neurol. 2016]Article
Filosto M, Author ; Filosto M ; Aureli M ; Castellotti B ; Rinaldi F ; Schiumarini D ; Valsecchi M ; Lualdi S ; Mazzotti R ; Pensato V ; Rota S ; Gellera C ; Filocamo M ; Padovani A | 2016Comment in: A new case of SMA phenotype without epilepsy due to biallelic variants in ASAH1. [Eur J Hum Genet. 2019]Article
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Francis A ; Sunitha B ; Vinodh K ; Polavarapu K ; Katkam SK ; Modi SK ; Srinivas Bharath MM ; Gayathri N ; Nalini A ; Thangaraj K | 2014Article
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Kannan MA ; Challa S ; Urtizberea JA ; Krahn M ; Jabeen AS ; Borgohain R | 2012Accès au résumé PubMed / to PubMed abstractArticle
Srivastava NK ; Pradhan S ; Mittal B ; Gowda GAN | 2010Accès au résumé PubMed / to PubMed abstractArticle
Accès au résumé PubMed / to PubMed abstractArticle
Urtizberea JA ; Bassez G ; Leturcq F ; Nguyen K ; Krahn M | 09/2008Accès au résumé PubMed / to PubMed abstractArticle
Singhal BS ; Bhatia NS ; Umesh T ; Menon S | 09/2008Accès au résumé PubMed / to PubMed abstractArticle
Accès au résumé PubMed / to PubMed abstractArticle
Lakshmi R ; Viswanathan V ; Arthi C | 2008Duchenne and Becker muscular dystrophies are X-linked allelic disorders caused due to mutations in the DMD gene. Mutation detection is laborious due to the presence of 79 exons in the DMD gene and carrier analysis complicated due to the heterozy[...]Article
Purushottam M ; Ram Murthy A ; Shubha GN ; Gayathri N ; Nalini A | 2008Accès au résumé PubMed / to PubMed abstract