Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1.
about
Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order MennonitesAssignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13.Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutationsImproved prognosis for congenital nephrotic syndrome of the Finnish type in Irish families.Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q.Molecular and genetic basis of inherited nephrotic syndrome
P2860
Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Fine mapping and haplotype ana ...... yndrome on chromosome 19q13.1.
@ast
Fine mapping and haplotype ana ...... yndrome on chromosome 19q13.1.
@en
type
label
Fine mapping and haplotype ana ...... yndrome on chromosome 19q13.1.
@ast
Fine mapping and haplotype ana ...... yndrome on chromosome 19q13.1.
@en
prefLabel
Fine mapping and haplotype ana ...... yndrome on chromosome 19q13.1.
@ast
Fine mapping and haplotype ana ...... yndrome on chromosome 19q13.1.
@en
P2093
P2860
P1476
Fine mapping and haplotype ana ...... yndrome on chromosome 19q13.1.
@en
P2093
Kestailä M
Männikkö M
Peltonen L
Ryynänen M
Tryggvason K
P2860
P304
P407
P577
1995-12-01T00:00:00Z