Maternal mutations of FOXF1 cause alveolar capillary dysplasia despite not being imprinted.

about

Alveolar capillary dysplasia with misalignment of the pulmonary veins: clinical, histological, and genetic aspects

P2860

Q58713813-49ACF1D9-9722-4B01-B565-2EE3ABC94A2E

P2860

Maternal mutations of FOXF1 cause alveolar capillary dysplasia despite not being imprinted.

Item

http://www.wikidata.org/entity/Q52679444

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Maternal mutations of FOXF1 ca ...... a despite not being imprinted.

@en

Maternal mutations of FOXF1 ca ...... a despite not being imprinted.

@nl

type

Item

label

Maternal mutations of FOXF1 ca ...... a despite not being imprinted.

@en

Maternal mutations of FOXF1 ca ...... a despite not being imprinted.

@nl

prefLabel

Maternal mutations of FOXF1 ca ...... a despite not being imprinted.

@en

Maternal mutations of FOXF1 ca ...... a despite not being imprinted.

@nl

P1476

Maternal mutations of FOXF1 ca ...... a despite not being imprinted.

@en

P2093

Carlota Rovira Zurriaga

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

David Monk

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

Elisenda Moliner Calderon

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

Franck Court

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

Gudrun E Moore

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

Isabel Gazquez Serrano

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

Julio Moreno Hernando

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

Loreto Martorell

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

Luciana Rodiguez Guerineau

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

Miguel Alsina Casanova

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

P2860

Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations

Uniparental paternal disomy in Angelman's syndrome.

Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins

Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment.

Alveolar capillary dysplasia: a cause of persistent pulmonary hypertension of the newborn.

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

Human Oocyte-Derived Methylation Differences Persist in the Placenta Revealing Widespread Transient Imprinting.

Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder.

Paternal or Maternal Uniparental Disomy of Chromosome 16 Resulting in Homozygosity of a Mutant Allele Causes Fanconi Anemia

Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain.

P304

615-620

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

P31

scholarly article

P356

10.1002/HUMU.23213

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

P433

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

P478

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

P50

Ana Monteagudo-Sánchez

P577

2017-03-03T00:00:00Z

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

P698

28256047

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

Maternal mutations of FOXF1 cause alveolar capillary dysplasia despite not being imprinted.

about

P2860

P2860

Maternal mutations of FOXF1 cause alveolar capillary dysplasia despite not being imprinted.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698