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Database ID
RNA ID
RNA Type
Disease Type
Disease Category
Sample Source
GEO ID
Detail
exR0075526
KCNV2
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0075527
KCP
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0075528
KCTD1
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0075529
KCTD10
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0075530
KCTD11
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0075531
KCTD12
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0075532
KCTD13
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0075533
KCTD14
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0075534
KCTD15
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0075535
KCTD16
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0075536
KCTD17
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0075537
KCTD18
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0075538
KCTD19
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0075539
KCTD2
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0075540
KCTD20
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail

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