Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Laufer, Benjamin I"'
Autor:
Laufer, Benjamin I, Hwang, Hyeyeon, Jianu, Julia M, Mordaunt, Charles E, Korf, Ian F, Hertz-Picciotto, Irva, LaSalle, Janine M
Publikováno v:
Human molecular genetics, vol 29, iss 21
Neonatal dried blood spots (NDBS) are a widely banked sample source that enables retrospective investigation into early life molecular events. Here, we performed low-pass whole genome bisulfite sequencing (WGBS) of 86 NDBS DNA to examine early life D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4b08edfa89e3cd1dcd42a562616af005
https://escholarship.org/uc/item/0n50z6b7
https://escholarship.org/uc/item/0n50z6b7
Autor:
Laufer, Benjamin I, Hwang, Hyeyeon, Vogel Ciernia, Annie, Mordaunt, Charles E, LaSalle, Janine M
Publikováno v:
Epigenetics, vol 14, iss 7
Down Syndrome (DS) is the most common genetic cause of intellectual disability, in which an extra copy of human chromosome 21 (HSA21) affects regional DNA methylation profiles across the genome. Although DNA methylation has been previously examined a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::d0c157a2a59152836f5a00cb96604b58
https://escholarship.org/uc/item/6sg1q4fp
https://escholarship.org/uc/item/6sg1q4fp