H.E. Shamseldin

Type de document

Co-auteur

L.J. Ying

I. Xenarios

C.F. Wright

M. Wiederkehr

N. Voisin

P.M. van Hasselt

G. van Haaften

E.M. Schindewolf

D. Sanlaville

B. Roechert

A. Reymond

B. Reversade

A. Putoux

E. Preiksaitiene

S. Pradervand

T. Pippucci

G.R. Monroe

G. Lesca

A. Lai

W. Kurdi

V. Kučinskas

S.S. Jamuar

M. Hashem

L. Guibaud

N. Guex

L. Guéneau

R.J. Fish

J. Delafontaine

L. Cimbalistienė

J. Chelly

C. Bonnard

Q. Ambusaidi

L. Ambrozaityte

F. Allias

F.S. Alkuraya

Date

Source

Serveur académique Lausannois (1)

Mot-clé

nourisson (1) gène (1) fruit (1) enfant (1) Development (1) Defects (1) Causative (1) Aspect (1) Cases (1) Genes (1) Toes (1) Syndactyly (1) Muscle hypotonia (1) Mice (1) Human beings (1) Magnetic resonance imaging (1) Life (1) Hydrocephalus (1) Fruit (1) Flies (1) Families (1) Defects (1) Clubfoot (1) Cataract (1) Brain stem (1) Brain (1) Arthrogryposis (1) Animals (1) Cases (1) Embryos (1)

Documents écrit par H.E. Shamseldin (1) | parle de H.E. Shamseldin (0)

KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis.

L. Gueneau et al. (4 janv. 2018)