Microarray oligonucleotide probe designer (MOPeD): A web service
about
Disruption of RAB40AL function leads to Martin--Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorderTargeted enrichment of genomic DNA regions for next-generation sequencingTargeted sequencing of the human X chromosome exome.Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse.
P2860
Microarray oligonucleotide probe designer (MOPeD): A web service
description
2010 nî lūn-bûn
@nan
2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Microarray oligonucleotide probe designer (MOPeD): A web service
@ast
Microarray oligonucleotide probe designer (MOPeD): A web service
@en
Microarray oligonucleotide probe designer
@nl
type
label
Microarray oligonucleotide probe designer (MOPeD): A web service
@ast
Microarray oligonucleotide probe designer (MOPeD): A web service
@en
Microarray oligonucleotide probe designer
@nl
prefLabel
Microarray oligonucleotide probe designer (MOPeD): A web service
@ast
Microarray oligonucleotide probe designer (MOPeD): A web service
@en
Microarray oligonucleotide probe designer
@nl
P2093
P2860
P356
P1476
Microarray oligonucleotide probe designer (MOPeD): A web service
@en
P2093
David J Cutler
Donna Martin
Jirair K Bedoyan
Kajari Mondal
Michael E Zwick
Vanessa L Horner
Viren C Patel
P2860
P304
P356
10.2147/OAB.S13741
P577
2010-11-01T00:00:00Z