Search Results - "Téllez García, Ana Laura"
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Genetics and environment in embryogenesis of sirenomelia sequence: case report
Published in Universidad Médica Pinareña (01-07-2020)“…Introduction: the sirenomelia sequence is a primary defect that occurs in the mesoderm of the posterior middle axis of the embryo and turns out the fusion of…”
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2
Genetics and environment in embryogenesis of sirenomelia sequence: case report
Published in Universidad Médica Pinareña (01-07-2020)“…Introduction: the sirenomelia sequence is a primary defect that occurs in the mesoderm of the posterior middle axis of the embryo and turns out the fusion of…”
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Journal Article -
3
Prenatal suspicion and postnatal diagnosis of a patient with cystic fibrosis
Published in Universidad Médica Pinareña (01-03-2019)“…Introduction: Cystic fibrosis is a genetic disease of autosomal recessive inheritance, characterized by dysfunction of the exocrine secretion glands. Case…”
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4
Prenatal suspicion and postnatal diagnosis of a patient with cystic fibrosis
Published in Universidad Médica Pinareña (01-03-2019)“…Introduction: Cystic fibrosis is a genetic disease of autosomal recessive inheritance, characterized by dysfunction of the exocrine secretion glands. Case…”
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Journal Article -
5
Genética y ambiente en la embriogénesis de la secuencia sirenomelia, reporte de un caso
Published in Universidad Médica Pinareña (2021)“…Introduction: the sirenomelia sequence is a primary defect that occurs in the mesoderm of the posterior middle axis of the embryo and turns out the fusion of…”
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6
Cardiopatía congénita y situs inverso como expresión prenatal del síndrome Ivemark
Published in Universidad Médica Pinareña (2019)“…Introduction: Ivemark Syndrome is a rare congenital condition that affects multiple organs of the body; it is classified as a disorder of heterotaxiaor…”
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7
Sospecha prenatal y diagnóstico postnatal de un paciente con fibrosis quística
Published in Universidad Médica Pinareña (2019)“…Introduction: Cystic fibrosis is a genetic disease of autosomal recessive inheritance, characterized by dysfunction of the exocrine secretion glands.Case…”
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8
Congenital heart disease and inverse situs as a prenatal expression of Ivemark Syndrome
Published in Universidad Médica Pinareña (01-01-2019)“…Introduction: Ivemark Syndrome is a rare congenital condition that affects multiple organs of the body; it is classified as a disorder of heterotaxiaor…”
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9
Congenital heart disease and inverse situs as a prenatal expression of Ivemark Syndrome
Published in Universidad Médica Pinareña (01-01-2019)“…Introduction: Ivemark Syndrome is a rare congenital condition that affects multiple organs of the body; it is classified as a disorder of heterotaxiaor…”
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Journal Article