MJM Nowaczyk

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

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

J.H. Caberg

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 MJM Nowaczyk (1) | parle de MJM Nowaczyk (0)

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

L. Pizzo et al.