نتایج جستجو برای: copy number variations
تعداد نتایج: 1355626 فیلتر نتایج به سال:
Journal:
:Genomics & Informatics
2012
Journal:
:Journal of Investigative Dermatology
2016
Journal:
:BMC Genomics
2016
Journal:
:Animal Production Science
2019
Journal:
:Clinical Case Reports
2020
Journal:
:The Annals of Applied Statistics
2012
Journal:
:Frontiers in Genetics
2018
Journal:
:Investigative Opthalmology & Visual Science
2011
Journal:
:Orphanet Journal of Rare Diseases
2011
2010
Hasmik Mkrtchyan
Madeleine Gross
Sophie Hinreiner
Anna Polytiko
Marina Manvelyan
Kristin Mrasek
Nadezda Kosyakova
Elisabeth Ewers
Heike Nelle
Thomas Liehr
Samarth Bhatt
Karen Thoma
Erich Gebhart
Sylvia Wilhelm
Raimund Fahsold
Marianne Volleth
Anja Weise
The discovery of copy number variations (CNV) in the human genome opened new perspectives in the study of the genetic causes of inherited disorders and the etiology of common diseases. Differently patterned instances of somatic mosaicism in CNV regions have been shown to be present in monozygotic twins and throughout different tissues within an individual. A single-cell-level investigation of C...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید