science
plus
.abes.fr
|
explorer
À propos de :
van Heyningen Veronica
Goto
Sponge
NotDistinct
Permalink
An Entity of Type :
foaf:Person
, within Data Space :
scienceplus.abes.fr
associated with source
document(s)
Type:
Person
New Facet based on Instances of this Class
Attributs
Valeurs
type
Person
name
van Heyningen Veronica
Heyningen Veronica van
van Heyningen V.
Heyningen V.van
personal mailbox
v.vanheyningen@hgu.mrc.ac.uk
familyName
van Heyningen
Heyningen
Given name
V.
V
Veronica
Veronica van
V.van
is
relates
of
http://hub.abes.fr/bmj/periodical/jmedgenet/2002/volume_39/issue_1/B3598D6B5DC17CBEE053120B220A90C5/authorship/5
http://hub.abes.fr/oup/periodical/hmg/1993/volume_2/issue_8/101093hmg281332/authorship/2
http://hub.abes.fr/oup/periodical/hmg/1998/volume_7/issue_10/101093hmg7101611/authorship/2
http://hub.abes.fr/oup/periodical/hmg/1999/volume_8/issue_1/101093hmg8111/authorship/16
http://hub.abes.fr/oup/periodical/hmg/1995/volume_4/issue_3/101093hmg43351/authorship/4
http://hub.abes.fr/oup/periodical/hmg/1993/volume_2/issue_3/101093hmg23259/authorship/7
http://hub.abes.fr/oup/periodical/hmg/1999/volume_8/issue_2/101093hmg82165/authorship/8
http://hub.abes.fr/oup/periodical/hmg/2002/volume_11/issue_10/101093hmg11101161/authorship/1
http://hub.abes.fr/bmj/periodical/jmedgenet/1997/volume_34/issue_3/B35966E226426AB5E053120B220AFD24/authorship/7
http://hub.abes.fr/bmj/periodical/jmg/2007/volume_44/issue_12/B3598D6B63CD7CBEE053120B220A90C5/authorship/1
http://hub.abes.fr/bmj/periodical/jmedgenet/1997/volume_34/issue_4/B35966E226526AB5E053120B220AFD24/authorship/5
http://hub.abes.fr/oup/periodical/mutage/1995/volume_10/issue_5/101093mutage105439/authorship/5
http://hub.abes.fr/oup/periodical/hmg/1993/volume_2/issue_2/101093hmg22115/authorship/7
http://hub.abes.fr/oup/periodical/hmg/2006/volume_15/issue_9/101093hmgddl064/authorship/15
http://hub.abes.fr/oup/periodical/hmg/1995/volume_4/issue_3/101093hmg43415/authorship/12
http://hub.abes.fr/oup/periodical/nar/1998/volume_26/issue_1/101093nar261259/authorship/3
http://hub.abes.fr/oup/periodical/hmg/2004/volume_13/issue_suppl2/101093hmgddh254/authorship/1
http://hub.abes.fr/oup/periodical/hmg/2002/volume_11/issue_1/101093hmg11133/authorship/8
http://hub.abes.fr/oup/periodical/hmg/2006/volume_15/issue_12/101093hmgddl127/authorship/15
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_19/101093hmg10192049/authorship/6
http://hub.abes.fr/oup/periodical/hmg/2009/volume_18/issue_6/101093hmgddp008/authorship/21
http://hub.abes.fr/bmj/periodical/jmedgenet/1995/volume_32/issue_6/B35966E224096AB5E053120B220AFD24/authorship/3
is
Author
of
Position Effect in Human Genetic Disease
Micronucleus frequencies in lymphoblastoid cell lines measured with the cytokinesis-block technique and flow cytometry
PAX6 in sensory development
Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome
DNA binding capacity of the WT1 protein is abolished by Denys—Drash syndrome WT1 point mutations
Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type I
Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype
EYA4, a Novel Vertebrate Gene Related to Drosophila Eyes Absent
Evidence that WT1 mutations in Denys — Drash syndrome patients may act in a dominant-negative fashion
Aniridia-associated translocations, DNase hypersensitivity, sequence comparison and transgenic analysis redefine the functional domain of PAX6
Dinucleotide repeat polymorphism at the D11S995 locus
The human PAX6 mutation database
Mechanisms of non-Mendelian inheritance in genetic disease
Domain disruption and mutation of the bZIP transcription factor, MAF,associated with cataract, ocular anterior segment dysgenesis and coloboma
Missense Mutations in the Most Ancient Residues of the PAX6 Paired Domain Underlie a Spectrum of Human Congenital Eye Malformations
Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome
Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes
Alternative Linked Data Documents:
ODE
Content Formats:
RDF
ODATA
Microdata
