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Younes Mokrab, PhD sur LinkedIn : #medlab
Younes Mokrab, PhD sur LinkedIn : #medlab

Ilse Feenstra, Lisenka E. L. M. Vissers, Ronald J. E - ppt download
Ilse Feenstra, Lisenka E. L. M. Vissers, Ronald J. E - ppt download

Lisenka VISSERS | PhD, Assistant Professor | Radboud University, Nijmegen |  RU | Department of Human Genetics | Research profile
Lisenka VISSERS | PhD, Assistant Professor | Radboud University, Nijmegen | RU | Department of Human Genetics | Research profile

Re-establishing a face-to-face forum for the rare disease research  community – Wellcome Connecting Science courses and conferences
Re-establishing a face-to-face forum for the rare disease research community – Wellcome Connecting Science courses and conferences

Bestuur VSOP
Bestuur VSOP

News – Solve-RD
News – Solve-RD

PhenoScore quantifies phenotypic variation for rare genetic diseases by  combining facial analysis with other clinical features using a  machine-learning framework | Nature Genetics
PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework | Nature Genetics

Donders Institute - Lisenka Vissers has been appointed Professor of  Translational #Genomics at Radboud university medical center/Radboud  University. Her field of expertise involves the study of #DNA errors  causing rare genetic diseases.
Donders Institute - Lisenka Vissers has been appointed Professor of Translational #Genomics at Radboud university medical center/Radboud University. Her field of expertise involves the study of #DNA errors causing rare genetic diseases.

Lisenka Vissers - Professor - Radboudumc | LinkedIn
Lisenka Vissers - Professor - Radboudumc | LinkedIn

Lisenka VISSERS | PhD, Assistant Professor | Radboud University, Nijmegen |  RU | Department of Human Genetics | Research profile - Page 3
Lisenka VISSERS | PhD, Assistant Professor | Radboud University, Nijmegen | RU | Department of Human Genetics | Research profile - Page 3

Un modèle informatique reconnaît 37 syndromes héréditaires à partir d'un  balayage facial - Le Spécialiste
Un modèle informatique reconnaît 37 syndromes héréditaires à partir d'un balayage facial - Le Spécialiste

PDF] Array-Based Comparative Genomic Hybridization for the Genomewide  Detection of Submicroscopic Chromosomal Abnormalities by Lisenka E.L.M.  Vissers, Bert B.A. de Vries, Kazutoyo Osoegawa, Irene M. Janssen, Ton  Feuth, Chik On Choy, Huub
PDF] Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal Abnormalities by Lisenka E.L.M. Vissers, Bert B.A. de Vries, Kazutoyo Osoegawa, Irene M. Janssen, Ton Feuth, Chik On Choy, Huub

Sequencing bij kinderen met genetische aandoeningen: van laatste redmiddel  naar spoedtest | ZonMw
Sequencing bij kinderen met genetische aandoeningen: van laatste redmiddel naar spoedtest | ZonMw

Hélène DEVINNE - Office Manager - Illumina | LinkedIn
Hélène DEVINNE - Office Manager - Illumina | LinkedIn

Lisenka VISSERS | PhD, Assistant Professor | Radboud University, Nijmegen |  RU | Department of Human Genetics | Research profile
Lisenka VISSERS | PhD, Assistant Professor | Radboud University, Nijmegen | RU | Department of Human Genetics | Research profile

A complex structural variant near SOX3 causes X-linked split-hand/foot  malformation
A complex structural variant near SOX3 causes X-linked split-hand/foot malformation

Solve-RD public symposium
Solve-RD public symposium

Lisenka Vissers appointed professor of Translational Genomics - Radboudumc
Lisenka Vissers appointed professor of Translational Genomics - Radboudumc

Lisenka VISSERS | PhD, Assistant Professor | Radboud University, Nijmegen |  RU | Department of Human Genetics | Research profile
Lisenka VISSERS | PhD, Assistant Professor | Radboud University, Nijmegen | RU | Department of Human Genetics | Research profile

Inaugurele rede Prof. Dr. Lisenka Vissers 'Het móét genetisch zijn'
Inaugurele rede Prof. Dr. Lisenka Vissers 'Het móét genetisch zijn'

De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA,  Cause Syndromic Intellectual Disability Resembli
De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembli

VISSERS Lisenka - React-congress
VISSERS Lisenka - React-congress

PhenoScore quantifies phenotypic variation for rare genetic diseases by  combining facial analysis with other clinical features using a  machine-learning framework | Request PDF
PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework | Request PDF

Lisenka Vissers (@LisenkaVissers) / X
Lisenka Vissers (@LisenkaVissers) / X

ZonMw
ZonMw

Samih Alqawlaq, PhD on LinkedIn: Medlab- Dubai, UAE: Illumina is hosting a  genomics workshop led by top…
Samih Alqawlaq, PhD on LinkedIn: Medlab- Dubai, UAE: Illumina is hosting a genomics workshop led by top…