(Q34423857)

2 August 2017

title

Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome (English)

1 reference

2 August 2017

1 reference

4

1 reference

2 August 2017

2

Lihadh Al-Gazali

1 reference

2 August 2017

10

Charles B Majoie

1 reference

2 August 2017

12

Raoul C Hennekam

1 reference

2 August 2017

Mariëlle Alders

1

1 reference

2 August 2017

Isabelle Cordeiro

3

1 reference

2 August 2017

Livia Garavelli

5

1 reference

2 August 2017

Beyhan Tuysuz

6

1 reference

2 August 2017

Faranak Salehi

7

1 reference

2 August 2017

Martin A Haagmans

8

1 reference

2 August 2017

Olaf R Mook

9

1 reference

2 August 2017

Marcel M Mannens

11

1 reference

2 August 2017

publication date

7 June 2014

1 reference

2 August 2017

1 reference

2 August 2017

volume

133

1 reference

2 August 2017

issue

9

1 reference

2 August 2017

page(s)

1161-1167

1 reference

Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Further delineation of Hennekam syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

CCBE1 is essential for mammalian lymphatic vascular development and enhances the lymphangiogenic effect of vascular endothelial growth factor-C in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

An evolutionary shift in the regulation of the Hippo pathway between mice and flies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Next-generation sequencing demands next-generation phenotyping

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Ccbe1 is required for embryonic lymphangiogenesis and venous sprouting

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Expression of vascular endothelial growth factor receptor-3 mRNA in the developing rat cerebellum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Prox1 regulates the notch1-mediated inhibition of neurogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

VEGF-C is a trophic factor for neural progenitors in the vertebrate embryonic brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Characterization of a Dchs1 mutant mouse reveals requirements for Dchs1-Fat4 signaling during mammalian development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Angiopoietin-2 regulates cortical neurogenesis in the developing telencephalon

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Loss of Fat4 disrupts PCP signaling and oriented cell division and leads to cystic kidney disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Planar cell polarity protein Celsr1 regulates endothelial adherens junctions and directed cell rearrangements during valve morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Lymphedema-lymphangiectasia-mental retardation (Hennekam) syndrome: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome?

21 January 2018

2 references

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

21 January 2018

https://pubmed.ncbi.nlm.nih.gov/24913602

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-014-1456-Y

Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 Mutations

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24913602

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00439-014-1456-Y

1 reference

Dimensions Publication ID

2 August 2017

1021332241

0 references

1 reference