(Q34110177)

31 July 2017

0 references

CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricle (English)

1 reference

31 July 2017

0 references

1

Elizabeth Goldmuntz

1 reference

31 July 2017

Richard Bamford

2

1 reference

31 July 2017

Jayaprakash D Karkera

3

1 reference

31 July 2017

June dela Cruz

4

1 reference

31 July 2017

Erich Roessler

5

1 reference

31 July 2017

Maximilian Muenke

6

1 reference

31 July 2017

language of work or name

English

0 references

publication date

17 January 2002

1 reference

American Journal of Human Genetics

31 July 2017

published in

1 reference

31 July 2017

volume

70

1 reference

31 July 2017

issue

3

1 reference

31 July 2017

page(s)

776-780

1 reference

Nodal signals to Smads through Cripto-dependent and Cripto-independent mechanisms

31 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384955

Left-right asymmetry and cardiac looping: implications for cardiac development and congenital heart disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384955

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384955

The EGF-CFC gene family in vertebrate development.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384955

Conserved requirement for EGF-CFC genes in vertebrate left-right axis formation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384955

X-linked situs abnormalities result from mutations in ZIC3

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384955

A differential display strategy identifies Cryptic, a novel EGF-related gene expressed in the axial and lateral mesoderm during mouse gastrulation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384955

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384955

Congenital heart disease: prevalence at livebirth. The Baltimore-Washington Infant Study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384955

X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384955

A role of the cryptic gene in the correct establishment of the left-right axis.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384955

The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384955

Occurrence of cardiac malformations in relatives of children with transposition of the great arteries

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384955

Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study

9 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11799476

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Frequency of 22q11 deletions in patients with conotruncal defects

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11799476

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/339079

1 reference

31 July 2017

1 reference

31 July 2017

1 reference