J.H. Caberg

Type de document

Co-auteur

S. Zeesman

J. Yoon

E. Voorhoeve

M. Vincent

A. Van Dijck

P. Stankiewicz

C. Skinner

E. Sistermans

C. Schwartz

J.A. Rosenfeld

C. Romano

A. Reymond

A. Renieri

P. Prontera

K. Pope

A. Polyak

L. Pizzo

O. Pichon

C. Perrine

D. Pazuchanics

MJM Nowaczyk

M. Nizon

A.L. Mosca-Boidron

S. Mercier

E. McCready

T. Mattina

D. Martin-Coignard

N. Marle

F. Mari

K. Männik

L. Mandarà

M., . Lefebvre

C. Le Caignec

V Kumar

A. Krishnan

R.F. Kooy

B. Keren

R.L. Kember

M. Jensen

B. Isidor

E. HUBER

S. Girirajan

O. Galesi

M. Fichera

L. Faivre

A. Curró

S.W. Cheung

L. Castiglia

P. Callier

M. Bucan

S. Blesson

C. Beneteau

E. Avola

J. Andrieux

D.J. Amor

Source

Serveur académique Lausannois (1)

Mot-clé

mise sous écran protecteur (1) information (1) histoire (1) évaluation (1) ADN (1) maladie (1) Deletion (1) History (1) Genealogy (1) Phenotype (1) Genetic disorders--Diagnosis (1) Genes (1) Cell adhesion molecules (1) Will (1) Strong family (1) Parents (1) Nerve tissue (1) Human beings (1) Human chromosome abnormalities--Diagnosis (1) History (1) Head (1) Gene expression (1) Expression (1) Evaluation (1) DNA (1) Chromosomes (1) Carrier family (1) Brothers and sisters (1) Autism (1) Disabilities (1)

Documents écrit par J.H. Caberg (1) | parle de J.H. Caberg (0)

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.

L. Pizzo et al.