Alternate Title: Chromosome analysis of 303 pregnancy losses in Mexico. (English)

المؤلفون: Garduño-Zarazúa, Luz M., Mayén, Dora G., Meléndez-Hernández, Ricardo, Paz-Martínez, Antonio J., Ramírez-Arroyo, Eva, Sosa, David, Aguinaga, Mónica, Pérez-Durán, Javier, Ríos, Osiris, López-Valdez, Jaime, Torres, Leda, Frías, Sara

المصدر: Gaceta Médica de México; ene/feb2024, Vol. 160 Issue 1, p81-91, 11p

المؤلفون: López‐Félix, Jana, Flores‐Gallegos, Leticia, Garduño‐Zarazúa, Luz, Leis‐Márquez, Teresa, Juárez‐García, Luz, Meléndez‐Hernández, Ricardo, Castelazo‐Morales, Ernesto, Mayén‐Molina, Dora

المصدر: Clinical Case Reports; Jun2017, Vol. 5 Issue 6, p986-992, 7p

مصطلحات موضوعية: TRISOMY, PRENATAL diagnosis, PREGNANCY, COUNSELING, CYTOGENETICS, DIAGNOSIS

Alternate Title: Non invasive prenatal test (NIPT) in maternal blood by parallel massive sequencing. Initial experience in Mexican women and literature review. (English)

المؤلفون: Hernández-Gómez, Mariana, Meléndez-Hernández, Ricardo, Ramírez-Arroyo, Eva, Garduño-Zarazúa, Luz María, Mayén-Molina, Dora Gilda

المصدر: Ginecología y Obstetricia de México; may2015, Vol. 83 Issue 5, p277-288, 12p, 2 Charts

مصطلحات موضوعية: ANEUPLOIDY, PRENATAL genetic testing, PRENATAL diagnosis, NONINVASIVE diagnostic tests, DNA analysis, WOMEN, DIAGNOSTIC sex determination, MEDICAL care

مصطلحات جغرافية: MEXICO

Alternate Title: Recurrent aneuploidy in first trimester gestational loss: a case report and review of the literature. (English)

المؤلفون: Hernández-Gómez, Mariana, Meléndez-Hernández, Ricardo, Rojas-Saiz, Walter H., Maya-Goldsmit, Dan, Mayén-Molina, Dora Gilda

المصدر: Ginecología y Obstetricia de México; dic2013, Vol. 81 Issue 12, p733-737, 5p, 5 Diagrams

مصطلحات موضوعية: ANEUPLOIDY, RECURRENT miscarriage, TRISOMY, PREGNANCY in middle age, FOLLICLE-stimulating hormone, GENETICS, DISEASE risk factors, RISK factors in miscarriages

عنوان ترانسليتريتد: Estudio cromosómico de 303 pérdidas gestacionales en México.

المؤلفون: Garduño-Zarazúa LM; Applied Genetics Unit, Hospital Ángeles Lomas, Huixquilucan, State of Mexico.; Human Genetics Medical Research Unit, High Specialty Medical Unit, Hospital de Pediatría, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City.; Biomedical Sciences Doctorate Program, Universidad Nacional Autónoma de México, Mexico City., Mayén DG; Applied Genetics Unit, Hospital Ángeles Lomas, Huixquilucan, State of Mexico., Meléndez-Hernández R; Applied Genetics Unit, Hospital Ángeles Lomas, Huixquilucan, State of Mexico., Paz-Martínez AJ; Applied Genetics Unit, Hospital Ángeles Lomas, Huixquilucan, State of Mexico., Ramírez-Arroyo E; Applied Genetics Unit, Hospital Ángeles Lomas, Huixquilucan, State of Mexico., Sosa D; Applied Genetics Unit, Hospital Ángeles Lomas, Huixquilucan, State of Mexico., Aguinaga M; Department of Genetics, Instituto Nacional de Perinatología, Mexico City., Pérez-Durán J; Department of Reproductive and Perinatal Health Research, Instituto Nacional de Perinatología, Mexico City., Ríos O; Citogenetics Laboratory, Instituto Nacional de Pediatría, Mexico City., López-Valdez J; Department of Genetics, Hospital Centenario Miguel Hidalgo, Aguascalientes, Aguascalientes.; Woman's Hospital, Instituto de Salud del Estado de Aguascalientes, Aguascalientes., Torres L; Citogenetics Laboratory, Instituto Nacional de Pediatría, Mexico City., Frias S; Citogenetics Laboratory, Instituto Nacional de Pediatría, Mexico City.; Department of Genomic Medicine and Environmental Toxicology, Institute of Biomedical Research, Universidad Nacional Autónoma de México, Mexico City. Mexico.

المصدر: Gaceta medica de Mexico [Gac Med Mex] 2024; Vol. 160 (1), pp. 76-85.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Unidad de Congresos del Centro Médico Nacional Country of Publication: Mexico NLM ID: 0010333 Publication Model: Print Cited Medium: Internet ISSN: 0016-3813 (Print) Linking ISSN: 00163813 NLM ISO Abbreviation: Gac Med Mex Subsets: MEDLINE

مواضيع طبية MeSH: Abortion, Spontaneous*/epidemiology , Abortion, Spontaneous*/genetics , Karyotyping*/methods , Chromosome Aberrations* , In Situ Hybridization, Fluorescence*, Humans ; Female ; Mexico/epidemiology ; Pregnancy ; Stillbirth/genetics ; Stillbirth/epidemiology ; Adult ; Cytogenetic Analysis/methods ; Microsatellite Repeats ; Polymorphism, Single Nucleotide ; Young Adult

عنوان ترانسليتريتد: Prueba prenatal no invasiva (NIPT) en sangre materna a través de secuenciación masiva paralela (MPS). Experiencia inicial en mujeres mexicanas y revisión de la bibliografía.

المؤلفون: Hernández-Gómez M, Ramirez-Arroyo E, Meléndez-Hernández R, Garduño-Zaraza LM, Mayén-Molina DG

المصدر: Ginecologia y obstetricia de Mexico [Ginecol Obstet Mex] 2015 May; Vol. 83 (5), pp. 277-88.

نوع المنشور: English Abstract; Journal Article; Review

بيانات الدورية: Publisher: Asociación Mexicana de Ginecología y Obstetricia Country of Publication: Mexico NLM ID: 0376552 Publication Model: Print Cited Medium: Print ISSN: 0300-9041 (Print) Linking ISSN: 03009041 NLM ISO Abbreviation: Ginecol Obstet Mex Subsets: MEDLINE

مواضيع طبية MeSH: High-Throughput Nucleotide Sequencing/*methods , Prenatal Diagnosis/*methods , Trisomy/*diagnosis, Adult ; Aneuploidy ; Female ; Humans ; Mexico ; Middle Aged ; Pregnancy ; Prospective Studies ; Sex Determination Analysis/methods ; Young Adult

عنوان ترانسليتريتد: Aneuploidía recurrente en pérdida gestacional del primer trimestre: reporte de un caso y revisión de la bibliografía.

المؤلفون: Hernández-Gómez M, Meléndez-Hernández R, Rojas-Saiz WH, Maya-Goldsmit D, Mayén-Molina DG

المصدر: Ginecologia y obstetricia de Mexico [Ginecol Obstet Mex] 2013 Dec; Vol. 81 (12), pp. 733-7.

نوع المنشور: Case Reports; Journal Article; Review

بيانات الدورية: Publisher: Asociación Mexicana de Ginecología y Obstetricia Country of Publication: Mexico NLM ID: 0376552 Publication Model: Print Cited Medium: Print ISSN: 0300-9041 (Print) Linking ISSN: 03009041 NLM ISO Abbreviation: Ginecol Obstet Mex Subsets: MEDLINE

مواضيع طبية MeSH: Abortion, Spontaneous/*genetics , Chromosome Disorders/*genetics , Trisomy/*genetics, Adult ; Aneuploidy ; Chromosomes, Human, Pair 13/genetics ; Chromosomes, Human, Pair 18/genetics ; Female ; Follicle Stimulating Hormone, Human/blood ; Humans ; Maternal Age ; Middle Aged ; Pregnancy ; Pregnancy Trimester, First ; Recurrence ; Risk Factors ; Trisomy 13 Syndrome ; Trisomy 18 Syndrome