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Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy.
J Am Coll Cardiol. 2018 Nov 13;72(20):2457-2467. doi: 10.1016/j.jacc.2018.10.001.
J Am Coll Cardiol. 2018.
PMID: 30442288
Free article.
[A new mutation in the ALDH3A2 gene in a boy with Sjogren-Larsson syndrome].
Mora-Lopez F, Vilches-Moreno M, Marin-Iglesias R.
Mora-Lopez F, et al. Among authors: marin iglesias r.
Rev Neurol. 2018 Nov 16;67(10):415-416.
Rev Neurol. 2018.
PMID: 30403285
Free article.
Spanish.
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A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome.
Ley Martos M, Salado Reyes MJ, Marín Iglesias R, Gutiérrez Moro C, Lubián Gutiérrez M, Estepa Pedregosa L.
Ley Martos M, et al. Among authors: marin iglesias r.
J Mov Disord. 2020 Sep;13(3):229-231. doi: 10.14802/jmd.19071. Epub 2020 Jul 14.
J Mov Disord. 2020.
PMID: 32654475
Free PMC article.
No abstract available.
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[Health related problems as cause of visits to hospital emergency departments].
Baena Parejo MI, Faus Dáder MJ, Marín Iglesias R, Zarzuelo Zurita A, Jiménez Martín J, Martínez Olmos J.
Baena Parejo MI, et al. Among authors: marin iglesias r.
Med Clin (Barc). 2005 Feb 26;124(7):250-5. doi: 10.1157/13072035.
Med Clin (Barc). 2005.
PMID: 15743589
Spanish.
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What to consider when pseudohypoparathyroidism is ruled out: iPPSD and differential diagnosis.
Pereda A, Garin I; Spanish Network for Imprinting Disorders; Perez de Nanclares G.
Pereda A, et al.
BMC Med Genet. 2018 Mar 2;19(1):32. doi: 10.1186/s12881-018-0530-z.
BMC Med Genet. 2018.
PMID: 29499646
Free PMC article.
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