⚡ JavaScript disabled! ⚡
⚡ Unsupported browser! Works best in
modern browsers
. ⚡
Name
Last modified
Size
Parent Directory
2016 A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin–Goltz syndrome.docx
2016-08-17 08:41
809 KB
2018 Genetics of rotator cuff tears no association of col5a1 gene in a case-control study.pdf
2018-12-26 09:56
569 KB
2019 Case of Plasmodium knowlesi Malaria in Poland Linked to Travel in Southeast Asia.pdf
2020-03-18 08:51
438 KB
2020 Compound craniosynostosis, intellectual disability, and Noonan‐like facial dysmorphism associated with 7q32.3‐q35 deletion.pdf
2020-09-23 09:58
2307 KB
2020 Genetic factors in rotator cuff pathology potential influence of col 5A1 polymorphism in outcomes of rotator cuff repair.pdf
2020-05-21 03:35
519 KB
2020 Mitochondrial DNA Survey Reveals the Lack of Accuracy in Maremmano Horse Studbook Records.pdf
2020-09-30 02:27
1922 KB
2020 Non‐syndromic anophthalmia microphthalmia can be caused by a PORCN variant inherited in X‐linked recessive manner.pdf
2021-01-19 07:16
1743 KB
2021 Associations of site-specific CD4+-T-cell hypomethylation within CD40-ligand promotor and enhancer regions with disease activity of women with systemic lupus erythematosus.pdf
2022-05-03 08:54
379 KB
2021 Non-syndromic anophthalmiamicrophthalmia can be causedNon-syndromic anophthalmiamicrophthalmia can be caused by a PORCN variant inherited in X-linked recessive manner.pdf
2022-05-03 09:08
1743 KB
2021 Population-based carrier screening and prenatal diagnosis of fragile X syndrome in East Asian populations.pdf
2022-05-03 09:45
1836 KB
2022 Performance evaluation of three DNA sample tracking tools in a whole exome sequencing workflow.pdf
2022-05-03 07:50
2220 KB