Raul E. Aguilar-Pina
Mexico, MEX 03100, Mexico
Last Updated: 09/26/2026
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Found 28 publications
Rare germline disorders implicate long non-coding RNAs disrupted by chromosomal structural rearrangements.
Journal: medRxiv : the preprint server for health sciences
Published: July 01, 2024
Chromosomal structural rearrangements implicate long non-coding RNAs in rare germline disorders.
Journal: Human genetics
Published: May 19, 2024
Resolving Breakpoints of Chromosomal Rearrangements at the Nucleotide Level Using Sanger Sequencing.
Resolving Breakpoints of Chromosomal Rearrangements at the Nucleotide Level Using Sanger Sequencing.
Journal: Current protocols in human genetics
Published: December 28, 2020
Genetic counseling for women with 45,X/46,XX mosaicism: Towards more personalized management.
Journal: European journal of medical genetics
Published: September 27, 2020
Oocyte maturation arrest produced by TUBB8 mutations: impact of genetic disorders in infertility treatment.
Journal: Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology
Published: February 18, 2020
Comprehensive clinically oriented workflow for nucleotide level resolution and interpretation in prenatal diagnosis of de novo apparently balanced chromosomal translocations in their genomic landscape.
Journal: Human genetics
Published: December 09, 2019
Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage.
Journal: American journal of human genetics
Published: August 16, 2019
A recurrent de novo mutation in ATP1A3 gene in a Mexican patient with alternating hemiplegia of childhood detected by massively parallel sequencing.
Journal: Boletin medico del Hospital Infantil de Mexico
Published: January 19, 2019
Natural-cycle in vitro fertilization (IVF) combined with in vitro maturation in infertile patients with polycystic ovarian syndrome (PCOS) requiring IVF.
Journal: Taiwanese journal of obstetrics & gynecology
Published: October 17, 2018
Colestasis por deficiencia de 3b-Δ5-C27-hidroxiesteroide deshidrogenasa en un paciente con alteración en la síntesis de ácidos biliares
Journal: Boletin medico del Hospital Infantil de Mexico
Published: September 26, 2018
Combined Preimplantation Genetic Testing for Aneuploidy and Monogenic Disease in a Mexican Family Affected by X-linked Hypohidrotic Ectodermal Dysplasia
Journal: Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion
Published: August 02, 2018
Last Updated: 09/26/2026