2012
Prenatal Diagnosis and Postnatal Followup of Partial Trisomy 13q and Partial Monosomy 10p: A Case Report and Review of the Literature
Wei Y, Gao X, Yan L, Xu F, Li P, Zhao Y. Prenatal Diagnosis and Postnatal Followup of Partial Trisomy 13q and Partial Monosomy 10p: A Case Report and Review of the Literature. Case Reports In Genetics 2012, 2012: 821347. PMID: 23133763, PMCID: PMC3485761, DOI: 10.1155/2012/821347.Peer-Reviewed Original ResearchNeonatal hypoxic-ischemic encephalopathyArray comparative genomic hybridizationPartial monosomy 10pHypoxic-ischemic encephalopathyEpisodes of apneaIntensive care unitWeeks of gestationPartial trisomyPrenatal diagnosisMild psychomotor retardationPartial trisomy 13qPostnatal followupIschemic encephalopathyNeonatal deathCare unitBirth weightCase reportFetal viabilityUltrasound examinationFetal karyotypingIntermittent convulsionsPostnatal findingsFurther abnormalitiesUltrasound monitoringPsychomotor retardation
1988
The frequency of aneuploidy in prenatally diagnosed congenital heart disease: An indication for fetal karyotyping
Copel J, Cullen M, Green J, Mahoney M, Hobbins J, Kleinman C. The frequency of aneuploidy in prenatally diagnosed congenital heart disease: An indication for fetal karyotyping. American Journal Of Obstetrics And Gynecology 1988, 158: 409-413. PMID: 3341415, DOI: 10.1016/0002-9378(88)90166-4.Peer-Reviewed Original ResearchConceptsCongenital heart diseaseHeart diseaseFetal heart diseaseFrequency of aneuploidyNeonatal careCardiac anomaliesFetal echocardiogramPediatric literatureFetal karyotypingParental counselingFetal bloodNonviable fetusClinic dataCase identificationChromosomal abnormalitiesFetusesDiseaseAbnormal chromosomesChromosome analysisEchocardiogramInfantsUteroWorkupAbnormalitiesAmniocentesis
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