Array CGH Analysis of Paired Blood and Tumor Samples from Patients with Sporadic Wilms Tumor

about

Array CGH Analysis of Paired Blood and Tumor Samples from Patients with Sporadic Wilms Tumor

Item

http://www.wikidata.org/entity/Q35759070

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Array CGH Analysis of Paired B ...... ents with Sporadic Wilms Tumor

@ast

Array CGH Analysis of Paired B ...... ents with Sporadic Wilms Tumor

@en

type

Item

label

Array CGH Analysis of Paired B ...... ents with Sporadic Wilms Tumor

@ast

Array CGH Analysis of Paired B ...... ents with Sporadic Wilms Tumor

@en

prefLabel

Array CGH Analysis of Paired B ...... ents with Sporadic Wilms Tumor

@ast

Array CGH Analysis of Paired B ...... ents with Sporadic Wilms Tumor

@en

P1476

Array CGH Analysis of Paired B ...... ents with Sporadic Wilms Tumor

@en

P2093

Elena Vallespín

http://www.w3.org/2001/XMLSchema#string

Fernando Regla Vargas

http://www.w3.org/2001/XMLSchema#string

GT-CSGP Working Group

http://www.w3.org/2001/XMLSchema#string

Hector N Seuanez

http://www.w3.org/2001/XMLSchema#string

Inmaculada Rueda-Arenas

http://www.w3.org/2001/XMLSchema#string

Lara Rodriguez-Laguna

http://www.w3.org/2001/XMLSchema#string

Leila Cabral de Almeida Cardoso

http://www.w3.org/2001/XMLSchema#string

María Palomares-Bralo

http://www.w3.org/2001/XMLSchema#string

Pablo Lapunzina

http://www.w3.org/2001/XMLSchema#string

Paulo Antonio Silvestre de Faria

http://www.w3.org/2001/XMLSchema#string

P2860

Wnt signaling pathways in urological cancers: past decades and still growing

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly

The pluripotent renal stem cell regulator SIX2 is activated in renal neoplasms and influences cellular proliferation and migration

Identification of proteins that interact with the central coiled-coil region of the human protein kinase NEK1

Wilms tumour histology is determined by distinct types of precursor lesions and not epigenetic changes

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism

A simple salting out procedure for extracting DNA from human nucleated cells

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

P304

e0136812

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1371/JOURNAL.PONE.0136812

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Victor Martínez-Glez

María Del Carmen Crespo

P577

2015-08-28T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

281373848

http://www.w3.org/2001/XMLSchema#string

P698

26317783

http://www.w3.org/2001/XMLSchema#string

P932

4552764

http://www.w3.org/2001/XMLSchema#string