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Biallelic sequence variants in INTS1 in patients with devel..:
Care 4 Rare Canada Consortium
;
Krall, Max
;
Htun, Stephanie
...
European Journal of Human Genetics. 27 (2019) 4 - p. 582-593 , 2019
Link:
https://doi.org/10.1038/s41431-018-0298-9
RT Journal T1
Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomalies
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_s41431-018-0298-9&Exemplar=1&LAN=DE A1 Care 4 Rare Canada Consortium A1 Krall, Max A1 Htun, Stephanie A1 Schnur, Rhonda E. A1 Brooks, Alice S. A1 Baker, Laura A1 de Alba Campomanes, Alejandra A1 Lamont, Ryan E. A1 Gripp, Karen W. A1 Schneidman-Duhovny, Dina A1 Innes, A. Micheil A1 Mancini, Grazia M. S. A1 Slavotinek, Anne M. PB Springer Science and Business Media LLC YR 2019 SN 1018-4813 SN 1476-5438 JF European Journal of Human Genetics VO 27 IS 4 SP 582 OP 593 LK http://dx.doi.org/https://doi.org/10.1038/s41431-018-0298-9 DO https://doi.org/10.1038/s41431-018-0298-9 SF ELIB - SuUB Bremen
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