Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sreelata B. Nair"'
Publikováno v:
Genes and Diseases, Vol 11, Iss 3, Pp 100998- (2024)
Externí odkaz:
https://doaj.org/article/70e71036932b4efcaed9618110ff2f2c
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-6 (2021)
Abstract Background Cornelia de Lange syndrome is a relatively uncommon disorder associated with multiple congenital anomalies/mental retardation of unknown etiology with its incidence varying from 1:10,000 to 1:50,000 live births in different popula
Externí odkaz:
https://doaj.org/article/62c600d405ef4e329d77b8a236519408
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-6 (2021)
Background Cornelia de Lange syndrome is a relatively uncommon disorder associated with multiple congenital anomalies/mental retardation of unknown etiology with its incidence varying from 1:10,000 to 1:50,000 live births in different population grou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c48173343ea830a2cea824794d7a88f9
https://doi.org/10.1186/s43042-021-00142-3
https://doi.org/10.1186/s43042-021-00142-3