about
Clinical and genetic characteristics of mexican patients with juvenile presentation of niemann-pick type C disease.Novel LIPA mutations in Mexican siblings with lysosomal acid lipase deficiencyBirth after human chorionic gonadotropin-primed oocyte in vitro maturation and fertilization with testicular sperm in a normo-ovulatory patient.A human reproductive approach to the study of infertility in chimpanzees: An experience at Leon's Zoological Park, MexicoWRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational ProspectsIntracytoplasmic sperm injection (ICSI) in small ruminants.The future of sperm-derived mRNAs.Mucopolysaccharidosis type II in a female carrying a heterozygous stop mutation of the iduronate-2-sulfatase gene and showing a skewed X chromosome inactivation.Acro-spondylo-pubic dysostosis associated with cataracts, microcephaly, and normal intelligence.A rapidly progressive defective spermatogenesis in a Mexican family affected by spino-bulbar muscular atrophy.[Colestasis por deficiencia de 3b-Δ5-C27-hidroxiesteroide deshidrogenasa en un paciente con alteración en la síntesis de ácidos biliares]Bringing together clinical embryology and basic reproduction around human cloningThe future of sperm-derived mRNAsY chromosome microdeletions in Mexican males of couples with idiopathic recurrent pregnancy lossAre Y chromosome microdeletions and recurrent pregnancy loss really associated?Genetic screening in the American Society for Reproductive Medicine's new guidelines on diagnostic evaluation of the infertile maleNasopalpebral lipoma-coloboma syndrome: clinical, radiological, and histopathological description of a novel sporadic caseExome sequencing identifies a de novo frameshift mutation in the imprinted gene ZDBF2 in a sporadic patient with Nasopalpebral Lipoma-coloboma syndromeOocyte maturation arrest produced by TUBB8 mutations: impact of genetic disorders in infertility treatment27 years of prenatal diagnosis for Huntington disease in the United Kingdom[Combined Preimplantation Genetic Testing for Aneuploidy and Monogenic Disease in a Mexican Family Affected by X-linked Hypohidrotic Ectodermal Dysplasia]Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent MiscarriageA recurrent de novo mutation in ATP1A3 gene in a Mexican patient with alternating hemiplegia of childhood detected by massively parallel sequencingNatural-cycle in vitro fertilization (IVF) combined with in vitro maturation in infertile patients with polycystic ovarian syndrome (PCOS) requiring IVF
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description
investigador
@es
researcher
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wetenschapper
@nl
name
Raúl E Piña-Aguilar
@en
Raúl E Piña-Aguilar
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type
label
Raúl E Piña-Aguilar
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Raúl E Piña-Aguilar
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prefLabel
Raúl E Piña-Aguilar
@en
Raúl E Piña-Aguilar
@nl
P31
P496
0000-0002-2043-4282