Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism. - Zouaghi, Yassine; Choudhary, Anbreen Mazhar; Irshad, Saba; Adamo, Michela; Rehman, Khaleeq ur; Fatima, Ambrin; Shahid, Mariam; Najmi, Nida; De Azevedo Correa, Fernanda; Habibi, Imen; Boizot, Alexia; Niederländer, Nicolas J.; et al. (BMC Genomics, 2024)