(Q28657716)

2

0 references

Julia Wynn

3

object named as

Julia Wynn

0 references

author name string

Lan Yu

1

0 references

Gemma L Carvill

4

0 references

Yee Him Cheung

5

0 references

Yufeng Shen

6

0 references

George B Mychaliska

7

0 references

Kenneth S Azarow

8

0 references

Timothy M Crombleholme

9

0 references

Dai H Chung

10

0 references

Douglas Potoka

11

0 references

Brad W Warner

12

0 references

Brian Bucher

13

0 references

Foong-Yen Lim

14

0 references

John Pietsch

15

0 references

Charles Stolar

16

0 references

Marc S Arkovitz

18

0 references

Heather Mefford

20

0 references

Wendy K Chung

Journal of Medical Genetics

21

0 references

language of work or name

English

0 references

publication date

March 2014

0 references

published in

0 references

volume

51

0 references

issue

3

0 references

page(s)

197-202

0 references

cites work

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

Fast and accurate short read alignment with Burrows-Wheeler transform

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

Crystal Structures of Multiple GATA Zinc Fingers Bound to DNA Reveal New Insights into DNA Recognition and Self-Association by GATA

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

GATA6 is essential for embryonic development of the liver but dispensable for early heart formation

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

The transcription factor GATA6 is essential for branching morphogenesis and epithelial cell differentiation during fetal pulmonary development

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

GATA6 regulates HNF4 and is required for differentiation of visceral endoderm in the mouse embryo

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

VMD: visual molecular dynamics

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

GATA-6: a zinc finger transcription factor that is expressed in multiple cell lineages derived from lateral mesoderm

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

GATA6 mutations cause a broad phenotypic spectrum of diabetes from pancreatic agenesis to adult-onset diabetes without exocrine insufficiency

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

De novo copy number variants are associated with congenital diaphragmatic hernia

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

De novo mutations in human genetic disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

GATA6 haploinsufficiency causes pancreatic agenesis in humans

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

A Gata6-Wnt pathway required for epithelial stem cell development and airway regeneration.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

Genetic aspects of human congenital diaphragmatic hernia

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

Left congenital diaphragmatic hernia, absent pericardium, and liver heterotopia: a case report and review

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

Single gene disorders associated with congenital diaphragmatic hernia

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

Overview of epidemiology, genetics, birth defects, and chromosome abnormalities associated with CDH.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

SLC5A9/SGLT4, a new Na+-dependent glucose transporter, is an essential transporter for mannose, 1,5-anhydro-D-glucitol, and fructose

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3955383

Congenital absence of the pericardium and its mimics.

3 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101989

Congenital absence of the left pericardium and diaphragmatic defect in sibs.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101989

First report of a de novo 18q11.2 microdeletion including GATA6 associated with complex congenital heart disease and renal abnormalities

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24385578