Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Samantha Issleb"'
Autor:
Abul Kalam Azad, Lindsay Yanakakis, Samantha Issleb, Jessica Turina, Kelli Drabik, Christina Bonner, Eve Simi, Andrew Wagner, Morry Fiddler, Rizwan Naeem
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-7 (2020)
Abstract Background Full or partial monosomy of chromosome (chr) 21 is a very rare abnormal cytogenetic finding. It is characterized by variable sizes and deletion breakpoints on the long arm (q) of chr 21 that lead to a broad spectrum of phenotypes
Externí odkaz:
https://doaj.org/article/8ad9111576624b69945fa87b8f5f5c34
Autor:
Jessica Turina, Lindsay Yanakakis, Kelli Drabik, Eve Simi, Abul Kalam Azad, Morry Fiddler, Andrew Wagner, Christina Bonner, Samantha Issleb, Rizwan Naeem
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-7 (2020)
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-7 (2020)
Background Full or partial monosomy of chromosome (chr) 21 is a very rare abnormal cytogenetic finding. It is characterized by variable sizes and deletion breakpoints on the long arm (q) of chr 21 that lead to a broad spectrum of phenotypes that incl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0d9f5d7e7b36c450f8a8ae8a3229304
https://doi.org/10.21203/rs.3.rs-39199/v2
https://doi.org/10.21203/rs.3.rs-39199/v2