Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism.
Zouaghi Y, Choudhary AM, Irshad S, Adamo M, Rehman KU, Fatima A, Shahid M, Najmi N, De Azevedo Correa F, Habibi I, Boizot A, Niederländer NJ, Ansar M, Santoni F, Acierno J, Pitteloud N.
Zouaghi Y, et al. Among authors: choudhary am.
BMC Genomics. 2024 Aug 14;25(1):787. doi: 10.1186/s12864-024-10598-3.
BMC Genomics. 2024.
PMID: 39143522
Free PMC article.