SISTEMA INTEGRAL DE INFORMACIÓN ACADÉMICA - PÚBLICO

Estandia-Ortega B.
(Autor externo)

Obras con ISBN:0
Documentos en revistas:8
Colaboraciones en Tesis:0
Patentes:0
Obras con ISBN:No hay obras de este autor.
Documentos en revistas:
1.- The Enigmatic Etiology of Oculo-Auriculo-Vertebral Spectrum (OAVS): An Exploratory Gene Variant Interaction Approach in Candidate Genes (2022)
 
2.- Screening of IRF6 Variants in Patients Subjected to Genetic Association Studies for Nonsyndromic Cleft Lip/Palate (2021)
 
3.- Predominance of dystrophinopathy genotypes in mexican male patients presenting as muscular dystrophy with a normal multiplex polymerase chain reaction DMD gene result: A study including targeted next-generation sequencing (2019)
 
4.- Expansion of the variable expression of Muenke syndrome: Hydrocephalus without craniosynostosis (2016)
 
5.- Germline Mutations in NKX2-5, GATA4, and CRELD1 are Rare in a Mexican Sample of Down Syndrome Patients with Endocardial Cushion and Septal Heart Defects (2015)
 
6.- Erratum to: Germline Mutations in NKX2-5, GATA4, and CRELD1 are Rare in a Mexican Sample of Down Syndrome Patients with Endocardial Cushion and Septal Heart Defects [Pediatric Cardiology, 36, (2015), 802-808, DOI:10.1007/s00246-014-1091-3] (2015)
 
7.- A patient with trisomy 13 mosaicism with an unusual skin pigmentary pattern and prolonged survival (2014)
 
8.- Molecular analysis of the PAX8 gene in a sample of Mexican patients with primary congenital hypothyroidism: Identification of the recurrent p.Arg31His mutation (2012)
 
Colaboraciones en Tesis:No hay tesis de este autor.
Patentes:No hay patentes de este autor.