Prenatal and postnatal chromosomal microarray analysis in 885 cases of various congenital heart defects

Purpose This study aimed to evaluate the prevalence of clinically significant (pathogenic and likely pathogenic) variants detected by chromosomal microarray (CMA) tests performed for prenatally and postnatally detected congenital heart defects. Methods A retrospective evaluation of CMA analyses over...

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Veröffentlicht in:	Archives of gynecology and obstetrics 2022-10, Vol.306 (4), p.1007-1013
Hauptverfasser:	Salzer-Sheelo, Liat, Polak, Uri, Barg, Ayelet, Kahana, Sarit, Yacobson, Shiri, Agmon-Fishman, Ifaat, Klein, Cochava, Matar, Reut, Rurman-Shahar, Noa, Sagi-Dain, Lena, Basel-Salmon, Lina, Maya, Idit, Sukenik-Halevy, Rivka
Format:	Artikel
Sprache:	eng
Schlagworte:	Chromosome Aberrations Chromosomes Congenital diseases Defects Endocrinology Female Genetic testing Genomes Gynecology Heart Heart Defects, Congenital - epidemiology Heart Defects, Congenital - genetics Human Genetics Humans Maternal-Fetal Medicine Medicine Medicine & Public Health Microarray Analysis Obstetrics Obstetrics/Perinatology/Midwifery Pediatrics Pregnancy Prenatal Diagnosis Retrospective Studies Ultrasonography, Prenatal
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