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Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family
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B. G. KINA Et Al. , "Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family," MOLECULAR GENETICS & GENOMIC MEDICINE , vol.12, no.1, 2024

KINA, B. G. Et Al. 2024. Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family. MOLECULAR GENETICS & GENOMIC MEDICINE , vol.12, no.1 .

KINA, B. G., Selcuki, N. F. T., Bahat, P. Y., USTA, A. T., AYDIN, S., Rahmioglu, N., ... TUNCER KILINÇ, F. N.(2024). Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family. MOLECULAR GENETICS & GENOMIC MEDICINE , vol.12, no.1.

KINA, Buşra Et Al. "Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family," MOLECULAR GENETICS & GENOMIC MEDICINE , vol.12, no.1, 2024

KINA, Buşra G. Et Al. "Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family." MOLECULAR GENETICS & GENOMIC MEDICINE , vol.12, no.1, 2024

KINA, B. G. Et Al. (2024) . "Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family." MOLECULAR GENETICS & 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 & GENOMIC MEDICINE}, year=2024}