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Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes

Ciliopathy GenesDevelopmental AnomalyDevelopmental BiologyGenetic DisorderGeneticsChromosomal Microarray AnalysisPathologyPrenatal DiagnosisGenomicsFetal Structural AnomaliesFetal NeurodevelopmentDisease Gene IdentificationMedicineEpigeneticsClinical Genetics