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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

Crossref DOI link: https://doi.org/10.1007/s00439-021-02406-9

Published Online: 2021-12-01

Published Print: 2022-01

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Al-Hamed, Mohamed H. https://orcid.org/0000-0002-7207-6122
Kurdi, Wesam

Khan, Rubina

Tulbah, Maha

AlNemer, Maha

AlSahan, Nada

AlMugbel, Maisoon

Rafiullah, Rafiullah

Assoum, Mirna

Monies, Dorota

Shah, Zeeshan

Rahbeeni, Zuhair

Derar, Nada

Hakami, Fahad

Almutairi, Gawaher

AlOtaibi, Afaf

Ali, Wafaa

AlShammasi, Amal

AlMubarak, Wardah

AlDawoud, Samia

AlAmri, Saja

Saeed, Bashayer

Bukhari, Hanifa

Ali, Mohannad

Akili, Rana

Alquayt, Laila

Hagos, Samia

Elbardisy, Hadeel

Akilan, Asma

Almuhana, Nora

AlKhalifah, Abrar

Abouelhoda, Mohamed

Ramzan, Khushnooda

Sayer, John A.

Imtiaz, Faiqa
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Text and Data Mining valid from 2021-12-01

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Article History

Received: 18 August 2021

Accepted: 26 November 2021

First Online: 1 December 2021

Declarations

:

: The authors have no conflicts of interest to declare.

: The study was approved by the Research Advisory Council at King Faisal Specialist Hospital and Research Centre (KFSH&RC), Riyadh, Saudi Arabia (RAC# 2211035).

: Informed consent was obtained from all individual participants included in the study.

: Not applicable.

: Not applicable.

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