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

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Figshare2024-08-18 更新2026-04-08 收录
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https://springernature.figshare.com/articles/dataset/Additional_file_2_of_Genome_sequencing_reveals_novel_causative_structural_and_single_nucleotide_variants_in_Pakistani_families_with_congenital_hypogonadotropic_hypogonadism/26698374
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资源简介:
Supplementary Material 2.
提供机构:
De Azevedo Correa, Fernanda; Boizot, Alexia; Choudhary, Anbreen Mazhar; Shahid, Mariam; Irshad, Saba; Najmi, Nida; Niederländer, Nicolas J.; Ansar, Muhammad; Fatima, Ambrin; Habibi, Imen; Rehman, Khaleeq ur; Adamo, Michela; Pitteloud, Nelly; Santoni, Federico; Acierno, James; Zouaghi, Yassine
创建时间:
2024-08-18
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