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Identification of novel genetic causes of Rett syndrome-like phenotypes by whole exome sequencing
Univ Minho, Sch Hlth Sci, Life & Hlth Sci Res Inst ICVS, Braga, Portugal.;ICVS 3Bs PT Govt Associate Lab, Braga, Portugal..
Mt Sinai Sch Med, Mindich Child Hlth & Dev Inst, Seaver Autism Ctr, Dept Psychiat, New York, NY USA.;Mt Sinai Sch Med, Mindich Child Hlth & Dev Inst, Seaver Autism Ctr, Dept Genet & Genom Sci, New York, NY USA..
Hosp Geral St Antonio, Oporto, Portugal..
Hosp Pediat Coimbra, Serv Genet Med, Coimbra, Portugal..
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2015 (English)In: International Journal of Developmental Neuroscience, ISSN 0736-5748, E-ISSN 1873-474X, Vol. 47, 99-99 p.Article in journal, Meeting abstract (Other academic) PublishedText
Place, publisher, year, edition, pages
2015. Vol. 47, 99-99 p.
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Medical Genetics Neurosciences
URN: urn:nbn:se:uu:diva-279217DOI: 10.1016/j.ijdevneu.2015.04.269ISI: 000366534600259PubMedID: 26531593OAI: oai:DiVA.org:uu-279217DiVA: diva2:908401
Joint Meeting of the 20th Biennial Meeting of the International-Society-for-Developmental-Neuroscience / 5th Annual NeuroDevNet Brain Development Conference, JUL 19-24, 2014, Montreal, CANADA
Available from: 2016-03-02 Created: 2016-02-29 Last updated: 2016-03-02Bibliographically approved

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Jonasson, IngerAmeur, AdamGyllensten, Ulf
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Department of Immunology, Genetics and PathologyScience for Life Laboratory, SciLifeLab
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