(Q55119415)

21 June 2018

title

Novel copy-number variants in a population-based investigation of classic heterotaxy. (English)

1 reference

21 June 2018

author

Aiyi Liu

5

1 reference

21 June 2018

James L. Mills

11

1 reference

21 June 2018

Paul Romitti

9

object named as

Paul A Romitti

1 reference

21 June 2018

Shannon L Rigler

1

1 reference

21 June 2018

Denise M Kay

2

1 reference

21 June 2018

Robert J Sicko

3

1 reference

21 June 2018

Ruzong Fan

4

1 reference

21 June 2018

Michele Caggana

6

1 reference

21 June 2018

Marilyn L Browne

7

1 reference

21 June 2018

Charlotte M Druschel

8

1 reference

21 June 2018

Lawrence C Brody

10

1 reference

21 June 2018

language of work or name

English

0 references

publication date

18 September 2014

1 reference

21 June 2018

published in

Genetics in Medicine

1 reference

21 June 2018

volume

17

1 reference

21 June 2018

issue

5

1 reference

21 June 2018

page(s)

348-357

1 reference

21 June 2018

Genetic dissection of ventral folding morphogenesis in mouse: embryonic visceral endoderm-supplied BMP2 positions head and heart.

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22 June 2018

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High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy

22 June 2018

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22 June 2018

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Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

22 June 2018

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22 June 2018

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22 June 2018

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Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations

22 June 2018

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Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly

22 June 2018

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The nomenclature, definition and classification of cardiac structures in the setting of heterotaxy

22 June 2018

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22 June 2018

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Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia

22 June 2018

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22 June 2018

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22 June 2018

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22 June 2018

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Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects

22 June 2018

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22 June 2018

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Missense mutations in CRELD1 are associated with cardiac atrioventricular septal defects

22 June 2018

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Consequences of knocking out BMP signaling in the mouse

22 June 2018

1 reference

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Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD

22 June 2018

1 reference

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

22 June 2018

1 reference

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Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIB

22 June 2018

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X-linked situs abnormalities result from mutations in ZIC3

22 June 2018

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Gtx: a novel murine homeobox-containing gene, expressed specifically in glial cells of the brain and germ cells of testis, has a transcriptional repressor activity in vitro for a serum-inducible promoter

22 June 2018

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White-black differences in cardiovascular malformations in infancy and socioeconomic factors. The Baltimore-Washington Infant Study Group

22 June 2018

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Outcome of 200 patients after an extracardiac Fontan procedure

22 June 2018

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Zebrafish Bmp4 regulates left-right asymmetry at two distinct developmental time points

13 August 2018

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Fgf signaling negatively regulates Nodal-dependent endoderm induction in zebrafish

13 August 2018

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Specific association of missense mutations in CRELD1 with cardiac atrioventricular septal defects in heterotaxy syndrome

13 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FGIM.2014.112

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21 January 2018

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Crossref

https://api.crossref.org/works/10.1038%2FGIM.2014.112

Familial transposition of the great arteries caused by multiple mutations in laterality genes

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FGIM.2014.112

The nomenclature, definition and classification of cardiac structures in the setting of heterotaxy

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5901701

Heterotaxy: associated conditions and hospital-based prevalence in newborns

30 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25232849

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/GIM.2014.112

1 reference

21 June 2018

Dimensions Publication ID

1052437273

0 references

Fatcat ID

release_vf35zltugrgvpd72n2gbqb5ixi

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/vf35zltugrgvpd72n2gbqb5ixi

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

5901701

1 reference

21 June 2018

PubMed publication ID

25232849

1 reference

21 June 2018