Additional file 2 of Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism

Additional file 2 of Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism

Supplementary Material 2.

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Bibliographische Detailangaben
Hauptverfasser: 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., Ansar, Muhammad, Santoni, Federico, Acierno, James, Pitteloud, Nelly
Format: Dataset
Sprache:eng
Schlagworte:
FOS: Biological sciences
Genetics
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Beschreibung
Zusammenfassung:Supplementary Material 2.
DOI:10.6084/m9.figshare.26698374