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Year | Number of Results |
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2006 | 1 |
2007 | 1 |
2019 | 1 |
2024 | 0 |
PubMed (cited) for id: 618494
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De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-Progressive Neurocognitive Syndrome.
Am J Hum Genet. 2019 Mar 7;104(3):542-552. doi: 10.1016/j.ajhg.2019.01.013. Epub 2019 Feb 28.
Am J Hum Genet. 2019.
PMID: 30827498
Free PMC article.
Polymicrogyria, cerebellar vermis hypoplasia, severe facial dysmorphism and cleft palate: a new syndrome?
Mosca AL, Laurent N, Guibaud L, Callier P, Thauvin-Robinet C, Mugneret F, Huet F, Grimaldi M, Gouyon JB, Sandre D, Faivre L.
Mosca AL, et al.
Eur J Med Genet. 2007 Jan-Feb;50(1):48-53. doi: 10.1016/j.ejmg.2006.08.002. Epub 2006 Sep 12.
Eur J Med Genet. 2007.
PMID: 17067864
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