María Asuncion Orera Clemente

A case of ring chromosome 22 with deletion of the 22q13.3 region associated with agenesis of the corpus callosum, fornix and septum pellucidum.

A FISH based prenatal diagnosis protocol.

Actualización del Síndrome Antifosfolípido.

An excess of chromosome 1 breakpoints in male infertility.

Aspectos genéticos de la Obesidad.

Bases Genéticas de la obesidad.

Caracterizacion metabólica del receptor de la Insulina de las células H-35.

Complex chromosome rearrangement in a case of assisted reproduction by IVF-ICSI.

Conceptos básicos de genética.

Congenital absence, abnormal shape and reduced size tooth as manifestation of same genetic defect.

Criterios de derivación a consulta de genética.

Dosimetría Biológica de las radiaciones ionizantes, mediante el estudio de alteraciones cromosómicas y micronúcleos.

Dosimetría Biológica.

Down Regulation and recovery of the insulin receptor in H-35 cells is protein and RNA synthesis dependent.

Factores de riesgo asociados a la edad paterna.

Familial Pitt-Rogers-Danks: two new cases.

Family history record and hereditary cancer risk perception according to NCI criteria in a Spanish medical oncology service: a retrospective study.

FISH análisis in patients with short stature.

Folate resistant Neural Tube defects associated to MTHFR A1298C mutation.

Genética de la Obesidad.

Genética de las enfermedades endocrinas.

Genética de las sobrecargas férricas.

Genética del control Endocrino.

Genética del crecimiento.

Genética del metabolismo de los folatos.

Hacia una medicina genómica.

I/D Polymorfism of angiotensin converting enzyme in a population of morbid obesity.

Inmunological abnormalities in primary APS evolving into SLE: 6 years follow up in women with repeat pregnancy loss.

Insulin induced gene 2 rs7566605 Single Nucleotide Variant and Global DNA Methylation Index levels are associated to weight loss in a personalized weight reduction program.

Isoenzimas y distribución de la adenilato cinasa y creatin cinasa en la médula adrenal bovina.

Isolated second trimester low HCG associated to complicated pregnancy.

Mecanismos hereditarios de la obesidad: Obesidad poligénica.

Molecular analysis of a gestation consisting of a complete hydatidiform mole and normal dizygotic twin.

Multilineage differentiation of K-562 sublines.

Multiple fetal malformations in a case of trisomy 7p15-ter and monosomy 11q23-ter.

NID2 and OXA9 promoter hypermethylation as biomarkers for prevention and early detection in oral cavity squamous cell carcinoma tissues and saliva.

Polydactyly in 22q11 syndrome: Should it be taken into account?.

Prenatal diagnosis of Bardet Biedl syndrome in a case of hiperecogenic kidneys: Clinical use of DNA sequencing.

Recomendaciones para el estudio genético de las parejas con alteraciones en la reproducción.

Recurrent non immune hydrops fetalis in parents with shared HLA DR and DQ.

Screening bioquímico prenatal.

Seguimiento del paciente con Síndrome de Down.

Seudohermafroditismo masculino con seminoma intraabdominal sangrante como causa excepcional de abdomen agudo.

Severe brain malformation associated to ring chromosome 22.

Síndrome de anticuerpos antifosfolípidos Asociación con abortos e infertilidad.

Strategies and outcomes in prenatal diagnosis.

The prevalence of antiphospholipids antibodies in 261 spanish women with recurrent spontaneous abortion.

Trisomy 21 with a paternal isochromosome 21q. due to a postzygotic misdivision.

X chromosome aneuploidy in peripheral blood lymphocytes of repeat abortion patients.