About: Anne-Claire Brehin

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Anne-Claire Brehin Goto Sponge NotDistinct Permalink

An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Brehin, Anne-Claire (1981-....) Brehin, Anne-Claire (1981-....) Brehin, Anne-Claire (1981-....)
Life Event	http://www.idref.fr/129406333/birth
preferred label	Brehin, Anne-Claire (1981-....)
name	Anne-Claire Brehin
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
isni:identifierValid	0000000357318821
Given name	Anne-Claire
familyName	Brehin
has biographical i...tion (Deprecated)	Titulaire d'une thèse de doctorat en Microbiologie et Virologie à l'Université de Paris 7, 2008
gender	female
ORCID iD	0000-0002-3399-9231
is sameAs of	Brehin, Anne-Claire (1981-....) Brehin, Anne-Claire (1981-....) Brehin, Anne-Claire (1981-....) Brehin, Anne-Claire (1981-....)
is Author of	http://www.sudoc.fr/129404985/id http://www.sudoc.fr/168819554/id http://www.sudoc.fr/189965029/id Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies Psychosocial Impact of Predictive Genetic Testing in Hereditary Heart Diseases: The PREDICT Study A Simple, Universal, and Cost-Efficient Digital PCR Method for the Targeted Analysis of Copy Number Variations Muscle metabolic remodelling patterns in Duchenne muscular dystrophy revealed by ultra-high-resolution mass spectrometry imaging Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patient Metabolic causes of nonimmune hydrops fetalis: A next-generation sequencing panel as a first-line investigation. Differentiation between Fabry disease and hypertrophic cardiomyopathy with cardiac T1 mapping http://www.sudoc.fr/247067490/id La protéine OAS3 de la voie interferon inhibe la réplication du virus chikungunya dans les cellules humaines Loss of Methylation at GNAS Exon A/B Is Associated With Increased Intrauterine Growth Exome sequencing identifies the first genetic determinants of sirenomelia in humans A case of Hajdu-Cheney syndrome associated with psoriatic rheumatism, two causes of acro-osteolysis Disentangling molecular and clinical stratification patterns in beta-galactosidase deficiency Gestational choriocarcinoma associated with a germline TP53 mutation Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical use When a maternal heterozygous mutation of the CYP24A1 gene leads to infantile hypercalcemia through a maternal uniparental disomy of chromosome 20 Prenatal diagnosis by trio exome sequencing in fetuses with ultrasound anomalies: A powerful diagnostic tool
is primary topic of	http://www.idref.fr/129406333
is Opponent of	http://www.sudoc.fr/230500307/id

Faceted Search & Find service v1.13.91 as of Aug 16 2018

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3229 as of May 14 2019, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (70 GB total memory)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software