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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

Title:	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
Authors:	Al-Hamed, Mohamed H.^{Aff1, Aff2, IDs00439021024069_cor1}; Kurdi, Wesam^Aff3; Khan, Rubina^Aff3; Tulbah, Maha^Aff3; AlNemer, Maha^Aff3; AlSahan, Nada^Aff3; AlMugbel, Maisoon^Aff3; Rafiullah, Rafiullah^Aff2; Assoum, Mirna^Aff2; Monies, Dorota^Aff1; Shah, Zeeshan^Aff1; Rahbeeni, Zuhair^Aff4; Derar, Nada^Aff4; Hakami, Fahad^Aff5; Almutairi, Gawaher^Aff3; AlOtaibi, Afaf^Aff2; Ali, Wafaa^Aff2; AlShammasi, Amal^Aff2; AlMubarak, Wardah^Aff3; AlDawoud, Samia^Aff3; AlAmri, Saja^Aff3; Saeed, Bashayer^Aff3; Bukhari, Hanifa^Aff3; Ali, Mohannad^Aff3; Akili, Rana^Aff1; Alquayt, Laila^Aff1; Hagos, Samia^Aff1; Elbardisy, Hadeel^Aff2; Akilan, Asma^Aff2; Almuhana, Nora^Aff2; AlKhalifah, Abrar^Aff2; Abouelhoda, Mohamed^Aff1; Ramzan, Khushnooda^Aff1; Sayer, John A.^{Aff6, Aff7, Aff8}; Imtiaz, Faiqa^{Aff1, Aff2, IDs00439021024069_cor35}
Source:	Human Genetics. 141(1):101-126
Database:	Springer Nature Journals