B. G. Kına Et Al. , "Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family," Molecular Genetics and Genomic Medicine , vol.12, no.1, 2024
Kına, B. G. Et Al. 2024. Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family. Molecular Genetics and Genomic Medicine , vol.12, no.1 .
Kına, B. G., Topbas Selcuki, N. F., Bahat, P. Y., Usta, A. T., Aydın, S., Rahmioglu, N., ... Tuncer, F. N.(2024). Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family. Molecular Genetics and Genomic Medicine , vol.12, no.1.
Kına, Buşra Et Al. "Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family," Molecular Genetics and Genomic Medicine , vol.12, no.1, 2024
Kına, Buşra G. Et Al. "Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family." Molecular Genetics and Genomic Medicine , vol.12, no.1, 2024
Kına, B. G. Et Al. (2024) . "Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family." Molecular Genetics and Genomic Medicine , vol.12, no.1.
@article{article, author={Buşra Gizem KINA Et Al. }, title={Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family}, journal={Molecular Genetics and Genomic Medicine}, year=2024}