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Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism.

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Title: Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism.
Authors: Zouaghi, Yassine1,2 (AUTHOR), Choudhary, Anbreen Mazhar3,4 (AUTHOR), Irshad, Saba3 (AUTHOR), Adamo, Michela1,2 (AUTHOR), Rehman, Khaleeq ur4 (AUTHOR), Fatima, Ambrin5 (AUTHOR), Shahid, Mariam6 (AUTHOR), Najmi, Nida7 (AUTHOR), De Azevedo Correa, Fernanda1,2 (AUTHOR), Habibi, Imen1,2 (AUTHOR), Boizot, Alexia1,2 (AUTHOR), Niederländer, Nicolas J.1,2 (AUTHOR), Ansar, Muhammad8,9 (AUTHOR), Santoni, Federico1,2,10 (AUTHOR), Acierno, James2 (AUTHOR), Pitteloud, Nelly1,2 (AUTHOR) nelly.pitteloud@chuv.ch
Source: BMC Genomics. 8/14/2024, Vol. 25 Issue 1, p1-9. 9p.
Database: Academic Search Ultimate
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  Data: Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism.
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  Data: <searchLink fieldCode="JN" term="%22BMC+Genomics%22">BMC Genomics</searchLink>. 8/14/2024, Vol. 25 Issue 1, p1-9. 9p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=179038924
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              Text: 8/14/2024
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