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Matthew A. Lines
University of Calgary - Calgary / Canada
Medical and Health Sciences / Medical Genetics
AD Scientific Index ID: 4924256
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Matthew A. Lines's MOST POPULAR ARTICLES
1-)
Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndromeJKJ Van Houdt, BA Nowakowska, SB Sousa, BDC Van Schaik, ...Nature genetics 44 (4), 445-449, 20122412012
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Haploinsufficiency of a spliceosomal GTPase encoded by EFTUD2 causes mandibulofacial dysostosis with microcephalyMA Lines, L Huang, J Schwartzentruber, SL Douglas, DC Lynch, ...The American Journal of Human Genetics 90 (2), 369-377, 20121902012
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Molecular genetics of Axenfeld–Rieger malformationsMA Lines, K Kozlowski, MA WalterHuman molecular genetics 11 (10), 1177-1187, 20021872002
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Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndromeRL Hood, MA Lines, SM Nikkel, J Schwartzentruber, C Beaulieu, ...The American Journal of Human Genetics 90 (2), 308-313, 20122022012
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Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld–Rieger syndrome and anterior segment dysgenesisFB Berry, MA Lines, JM Oas, T Footz, DA Underhill, PJ Gage, MA WalterHuman molecular genetics 15 (6), 905-919, 20061742006
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