Genomic Insights from a Deeply Phenotyped Highly Consanguineous Neurodevelopmental Disorders Cohort
Hosneara Akter,Md. Atikur Rahaman,Tamannyat Binte Eshaque,Nesrin Mohamed,Amirul Islam, Mehzabin Morshed, Zaha Shahin, Al Muhaimin, Arif Md. Foyzullah, Rabeya Akter Mim, Farjana Binta Omar, Md. Nahid Hasan,Dharana Satsangi, Nahid Ahmed,Abdullah Al Saba,Nargis Jahan,Md. Arif Hossen, Md. Ashadujjaman Mondol, Ahammad Sharif Sakib, Rezwana Kabir, Mohammod Shah Jahan Chowdhury, Nusrat Shams,Shireen Afroz,Shayla Imam Kanta, Sarwar Jahan Bhuiyan, Rabi Biswas, Shehzad Hanif,Richa Tambi,Nasna Nassir,Muhammad Mizanur Rahman,Jinjie Duan,Anders D. Borglum, Robed Amin,Mohammed Basiruzzaman, Md. Kamruzzaman,Shaoli Sarker,Marc Woodbury-Smith,K. M. Furkan Uddin,A. H. M. Nurun Nabi,Mohammed Uddin GENETICS IN MEDICINE（2025）
Key words
Chromosomal microarray,Exome sequencing,Genetic etiology,Neurodevelopmental disorders,Long-read genome sequencing
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