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Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy
Authors: Waldmueller, S.; Sakthivel, S.; Saadi, A. V.; Selignow, C.; Rakesh, P. G.; Golubenko, M.; Joseph, P. K.; Padmakumar, R.; Richard, P.; Schwartz, K.; Tharakan, J. M.; Rajamanickam, C.; Vosberg, H. P.
Date of Publication (YYYY-MM-DD): 2003-06
Title of Journal: J Mol Cell Cardiol
Volume: 35
Issue / Number: 6
Start Page: 623
End Page: 636
Document Type: Article
ID: 199081.0
Low-densitiy DNA microarrays are versatile tools to screen for known mutations in hypertrophic cardiomyopathy
Authors: Waldmüller, S.; Freund, P.; Mauch, S.; Toder, R.; Vosberg, H.P.
Date of Publication (YYYY-MM-DD): 2002
Title of Journal: Human Mutation
Volume: 19
Start Page: 560
End Page: 569
Document Type: Article
ID: 47115.0
Entries: 1-2  
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