Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Gilyazetdinov Kamil"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-19 (2021)
Abstract Background Large-scale genomic analyses have provided insight into the genetic complexity of short stature (SS); however, only a portion of genetic causes have been identified. In this study, we identified disease-causing mutations in a coho
Externí odkaz:
https://doaj.org/article/5e01a665786b47638a7fcc09fc02b5f4
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-19 (2021)
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-19 (2021)
Background Large-scale genomic analyses have provided insight into the genetic complexity of short stature (SS); however, only a portion of genetic causes have been identified. In this study, we identified disease-causing mutations in a cohort of Kor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94881c6dce60e4de05af8cf4a601d60d
https://pubmed.ncbi.nlm.nih.gov/34217350
https://pubmed.ncbi.nlm.nih.gov/34217350
Akademický článek
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Autor:
Kamil, Gilyazetdinov1,2 (AUTHOR), Yoon, Ju Young3 (AUTHOR), Yoo, Sukdong3 (AUTHOR), Cheon, Chong Kun2,3 (AUTHOR) chongkun@pusan.ac.kr
Publikováno v:
Orphanet Journal of Rare Diseases. 7/3/2021, Vol. 16 Issue 1, p1-19. 19p.
Publikováno v:
Hormone Research in Paediatrics; 2021 Supplement, Vol. 94, p1-445, 445p
Publikováno v:
Hormone Research in Paediatrics; Sep2012 Supplement, Vol. 78, p329-349, 21p