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Severe neurological abnormalities in a young boy with impaired thyroid hormone sensitivity due to a novel mutation in the MCT8 gene.
Hormones (Athens). 2017 Apr;16(2):194-199. doi: 10.14310/horm.2002.1733.
Hormones (Athens). 2017.
PMID: 28742507
Free article.
The modifier effect of the BDNF gene in the phenotype of the WAGRO syndrome.
Rodríguez-López R, Pérez JM, Balsera AM, Rodríguez GG, Moreno TH, García de Cáceres M, Serrano MG, Freijo FC, Ruiz JR, Angueira FB, Pérez PM, Estévez MN, Gómez EG.
Rodríguez-López R, et al. Among authors: angueira fb.
Gene. 2013 Mar 10;516(2):285-90. doi: 10.1016/j.gene.2012.11.073. Epub 2012 Dec 21.
Gene. 2013.
PMID: 23266638
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Three new patients with congenital unilateral facial nerve palsy due to chromosome 22q11 deletion.
Puñal JE, Siebert MF, Angueira FB, Lorenzo AV, Castro-Gago M.
Puñal JE, et al. Among authors: angueira fb.
J Child Neurol. 2001 Jun;16(6):450-2. doi: 10.1177/088307380101600614.
J Child Neurol. 2001.
PMID: 11417615
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