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[Sotos syndrome: a novel nonsense mutation in NSD1 gene, presenting with neonatal cutis laxa].
An Pediatr (Barc). 2011 Aug;75(2):129-33. doi: 10.1016/j.anpedi.2011.02.018. Epub 2011 Apr 8.
An Pediatr (Barc). 2011.
PMID: 21482210
Free article.
Spanish.
Long-term follow-up of a patient with primary hypomagnesaemia and secondary hypocalcaemia due to a novel TRPM6 mutation.
Esteban-Oliva D, Pintos-Morell G, Konrad M.
Esteban-Oliva D, et al.
Eur J Pediatr. 2009 Apr;168(4):439-42. doi: 10.1007/s00431-008-0767-1. Epub 2008 Jun 12.
Eur J Pediatr. 2009.
PMID: 18548273
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Transient type I 2nd-degree congenital atrioventricular block: A case report.
Roguera Sopena M, Esteban Oliva D, Ocaña Rico M, Coroleu Lletget W, Zientalska Fendonczuk AM.
Roguera Sopena M, et al. Among authors: esteban oliva d.
Arch Cardiol Mex. 2023 Feb 2;93(1):124-126. doi: 10.24875/ACM.22000146.
Arch Cardiol Mex. 2023.
PMID: 35917627
Free PMC article.
No abstract available.
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