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1دورية أكاديمية
المساهمون: Bursa Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., orcid:0000-0002-9802-0880, Temel, Şehime, AAG-8385-2021, 6507885442
مصطلحات موضوعية: Variants, Azoospermia, Genetics & heredity, Adult, Alleles, Animals, Cell cycle checkpoints, Homozygote, Humans, Infertility, male, Meiosis, Mice, Mutation, Phenotype, Proteins, Spermatogenesis, Spermatozoa, Testis, Turkey, Whole exome sequencing, Male Infertility, Y Chromosome, Meiosis 1 arresting protein, mouse, Protein, Allele, Article, Cryptozoospermia, Disease severity
وصف الملف: application/pdf
العلاقة: Makale - Uluslararası Hakemli Dergi; KUAP(T)-2014/36; American Journal of Human Genetics; Yurt içi; Yurt dışı; Sanayi; Wyrwoll, M. J. vd. (2020). "Bi-allelic mutations in M1AP are a frequent cause of meiotic arrest and severely impaired spermatogenesis leading to male infertility". American Journal of Human Genetics, 107(2), 342-351.; https://doi.org/10.1016/j.ajhg.2020.06.010Test; https://www.sciencedirect.com/scienceTest/article/pii/S0002929720301981; http://hdl.handle.net/11452/30096Test; 000558491800014; 2-s2.0-85088861386; 341; 351; 107
الإتاحة: https://doi.org/10.1016/j.ajhg.2020.06.010Test
http://hdl.handle.net/11452/30096Test
https://www.sciencedirect.com/scienceTest/article/pii/S0002929720301981 -
2دورية أكاديمية
المساهمون: Bursa Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., orcid:0000-0002-9802-0880, Temel, Şehime, AAG-8385-2021, 6507885442
مصطلحات موضوعية: Variants, Azoospermia, Genetics & heredity, Adult, Alleles, Animals, Cell cycle checkpoints, Homozygote, Humans, Infertility, male, Meiosis, Mice, Mutation, Phenotype, Proteins, Spermatogenesis, Spermatozoa, Testis, Turkey, Whole exome sequencing, Male Infertility, Y Chromosome, Meiosis 1 arresting protein, mouse, Protein, Allele, Article, Cryptozoospermia, Disease severity
وصف الملف: application/pdf
العلاقة: Makale - Uluslararası Hakemli Dergi; KUAP(T)-2014/36; American Journal of Human Genetics; Yurt içi; Yurt dışı; Sanayi; Wyrwoll, M. J. vd. (2020). "Bi-allelic mutations in M1AP are a frequent cause of meiotic arrest and severely impaired spermatogenesis leading to male infertility". American Journal of Human Genetics, 107(2), 342-351.; https://doi.org/10.1016/j.ajhg.2020.06.010Test; https://www.sciencedirect.com/scienceTest/article/pii/S0002929720301981; http://hdl.handle.net/11452/30096Test; 000558491800014; 2-s2.0-85088861386; 341; 351; 107
الإتاحة: https://doi.org/10.1016/j.ajhg.2020.06.010Test
http://hdl.handle.net/11452/30096Test
https://www.sciencedirect.com/scienceTest/article/pii/S0002929720301981
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