Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene
about
Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
name
Characterization of a novel ge ...... on as the Meckel syndrome gene
@ast
Characterization of a novel ge ...... on as the Meckel syndrome gene
@en
Characterization of a novel ge ...... on as the Meckel syndrome gene
@en-gb
Characterization of a novel ge ...... on as the Meckel syndrome gene
@nl
type
label
Characterization of a novel ge ...... on as the Meckel syndrome gene
@ast
Characterization of a novel ge ...... on as the Meckel syndrome gene
@en
Characterization of a novel ge ...... on as the Meckel syndrome gene
@en-gb
Characterization of a novel ge ...... on as the Meckel syndrome gene
@nl
prefLabel
Characterization of a novel ge ...... on as the Meckel syndrome gene
@ast
Characterization of a novel ge ...... on as the Meckel syndrome gene
@en
Characterization of a novel ge ...... on as the Meckel syndrome gene
@en-gb
Characterization of a novel ge ...... on as the Meckel syndrome gene
@nl
P2093
P356
P1433
P1476
Characterization of a novel ge ...... on as the Meckel syndrome gene
@en
P2093
L Peltonen
N Horelli-Kuitunen
P356
10.1006/GENO.1998.5612
P407
P577
1999-01-01T00:00:00Z