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A new overgrowth syndrome is due to mutations in RNF125.
Hum Mutat. 2014 Dec;35(12):1436-41. doi: 10.1002/humu.22689.
Hum Mutat. 2014.
PMID: 25196541
Co-inheritance of HNF1a and GCK mutations in a family with maturity-onset diabetes of the young (MODY): implications for genetic testing.
López-Garrido MP, Herranz-Antolín S, Alija-Merillas MJ, Giralt P, Escribano J.
López-Garrido MP, et al. Among authors: alija merillas mj.
Clin Endocrinol (Oxf). 2013 Sep;79(3):342-7. doi: 10.1111/cen.12050. Epub 2013 Apr 1.
Clin Endocrinol (Oxf). 2013.
PMID: 23009393
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[Recommendations for the diagnosis and follow up of the foetus and newborn child born to mothers with autoimmune thyroid disease].
Ares Segura S, Temboury Molina C, Chueca Guindulain MJ, Grau Bolado G, Alija Merillas MJ, Caimari Jaume M, Casano Sancho P, Moreno Navarro JC, Rial Rodríguez JM, Rodríguez Sánchez A; en representación del Grupo de trabajo de tiroides de la Sociedad Española de Endocrinología Pediátrica.
Ares Segura S, et al. Among authors: alija merillas mj.
An Pediatr (Engl Ed). 2018 Oct;89(4):254.e1-254.e7. doi: 10.1016/j.anpedi.2018.07.006. Epub 2018 Sep 1.
An Pediatr (Engl Ed). 2018.
PMID: 30177500
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