Lista de obras -

27 years of prenatal diagnosis for Huntington disease in the United Kingdom

scientific article published on 14 December 2018

A human reproductive approach to the study of infertility in chimpanzees: An experience at Leon's Zoological Park, Mexico

artículo científico publicado en 2016

A rapidly progressive defective spermatogenesis in a Mexican family affected by spino-bulbar muscular atrophy.

artículo científico publicado en 2016

A recurrent de novo mutation in ATP1A3 gene in a Mexican patient with alternating hemiplegia of childhood detected by massively parallel sequencing

scientific article published on 01 January 2019

Acro-spondylo-pubic dysostosis associated with cataracts, microcephaly, and normal intelligence.

artículo científico publicado en 2014

Are Y chromosome microdeletions and recurrent pregnancy loss really associated?

artículo científico publicado en 2009

Birth after human chorionic gonadotropin-primed oocyte in vitro maturation and fertilization with testicular sperm in a normo-ovulatory patient.

artículo científico publicado en 2016

Bringing together clinical embryology and basic reproduction around human cloning

scientific article published on 14 October 2008

Clinical and genetic characteristics of mexican patients with juvenile presentation of niemann-pick type C disease.

artículo científico publicado en 2014

Exome sequencing identifies a de novo frameshift mutation in the imprinted gene ZDBF2 in a sporadic patient with Nasopalpebral Lipoma-coloboma syndrome

artículo científico publicado en 2016

Genetic screening in the American Society for Reproductive Medicine's new guidelines on diagnostic evaluation of the infertile male

artículo científico publicado en 2013

Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage

scientific article published on 31 October 2019

Intracytoplasmic sperm injection (ICSI) in small ruminants.

artículo científico

Mucopolysaccharidosis type II in a female carrying a heterozygous stop mutation of the iduronate-2-sulfatase gene and showing a skewed X chromosome inactivation.

artículo científico publicado en 2012

Nasopalpebral lipoma-coloboma syndrome: clinical, radiological, and histopathological description of a novel sporadic case

scientific article published on 01 May 2013

Natural-cycle in vitro fertilization (IVF) combined with in vitro maturation in infertile patients with polycystic ovarian syndrome (PCOS) requiring IVF

artículo científico publicado en 2019

Novel LIPA mutations in Mexican siblings with lysosomal acid lipase deficiency

artículo científico publicado en 2015

Oocyte maturation arrest produced by TUBB8 mutations: impact of genetic disorders in infertility treatment

artículo científico publicado en 2020

Testicular somatic cell-like cells derived from embryonic stem cells induce differentiation of epiblasts into germ cells

artículo científico publicado en 2021

The future of sperm-derived mRNAs

artículo científico publicado en 2006

The future of sperm-derived mRNAs.

artículo científico publicado en 2006

WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects

artículo científico publicado en 2016

Y chromosome microdeletions in Mexican males of couples with idiopathic recurrent pregnancy loss

scientific article published on 09 April 2012

[Colestasis por deficiencia de 3b-Δ5-C27-hidroxiesteroide deshidrogenasa en un paciente con alteración en la síntesis de ácidos biliares]

artículo científico publicado en 2018

[Combined Preimplantation Genetic Testing for Aneuploidy and Monogenic Disease in a Mexican Family Affected by X-linked Hypohidrotic Ectodermal Dysplasia]

artículo científico publicado en 2018

Lista de obras de

27 years of prenatal diagnosis for Huntington disease in the United Kingdom

A human reproductive approach to the study of infertility in chimpanzees: An experience at Leon's Zoological Park, Mexico

A rapidly progressive defective spermatogenesis in a Mexican family affected by spino-bulbar muscular atrophy.

A recurrent de novo mutation in ATP1A3 gene in a Mexican patient with alternating hemiplegia of childhood detected by massively parallel sequencing

Acro-spondylo-pubic dysostosis associated with cataracts, microcephaly, and normal intelligence.

Are Y chromosome microdeletions and recurrent pregnancy loss really associated?

Birth after human chorionic gonadotropin-primed oocyte in vitro maturation and fertilization with testicular sperm in a normo-ovulatory patient.

Bringing together clinical embryology and basic reproduction around human cloning

Clinical and genetic characteristics of mexican patients with juvenile presentation of niemann-pick type C disease.

Exome sequencing identifies a de novo frameshift mutation in the imprinted gene ZDBF2 in a sporadic patient with Nasopalpebral Lipoma-coloboma syndrome

Genetic screening in the American Society for Reproductive Medicine's new guidelines on diagnostic evaluation of the infertile male

Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage

Intracytoplasmic sperm injection (ICSI) in small ruminants.

Mucopolysaccharidosis type II in a female carrying a heterozygous stop mutation of the iduronate-2-sulfatase gene and showing a skewed X chromosome inactivation.

Nasopalpebral lipoma-coloboma syndrome: clinical, radiological, and histopathological description of a novel sporadic case

Natural-cycle in vitro fertilization (IVF) combined with in vitro maturation in infertile patients with polycystic ovarian syndrome (PCOS) requiring IVF

Novel LIPA mutations in Mexican siblings with lysosomal acid lipase deficiency

Oocyte maturation arrest produced by TUBB8 mutations: impact of genetic disorders in infertility treatment

Testicular somatic cell-like cells derived from embryonic stem cells induce differentiation of epiblasts into germ cells

The future of sperm-derived mRNAs

The future of sperm-derived mRNAs.

WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects

Y chromosome microdeletions in Mexican males of couples with idiopathic recurrent pregnancy loss

[Colestasis por deficiencia de 3b-Δ5-C27-hidroxiesteroide deshidrogenasa en un paciente con alteración en la síntesis de ácidos biliares]

[Combined Preimplantation Genetic Testing for Aneuploidy and Monogenic Disease in a Mexican Family Affected by X-linked Hypohidrotic Ectodermal Dysplasia]