A. Nemeth

Type de document

Co-auteur

C. Xu

R. Quinton

N. Pitteloud

D. Pignatelli

L. Marino

M. Hauschild

C. Flück

L. Favre

A. A. Dwyer

D. Cassatella

J. Zhang

H. Yang

A.M. van der Sloot

G. Szinnai

G.P. Sykiotis

B.J. Stevenson

S. Sharif

F. A. Santoni

S. Santini

V. Popovic

F. Phan-Hug

S. Pekic

S. Pekic Djurdjevic

G.E. Papadakis

G. Papadakis

A. Paepe

N.J. Niederländer

J. Meylan

P. Maeder

X. Liu

J. Li

J.R. Lemke

M. Lang-Muritano

L'Allemand, D.

D. Konrad

Ö.T. Iyidir

S.R. Howard

I. Halperin

C. Geyter

J.M. Ferrara

K. Feller

L. Dunkel

W.S. Dhillo

C. De Geyter

C. Chambion

P.M. Bouloux

D. Bartholdi

J.S. Acierno

J. Acierno

Source

Serveur académique Lausannois (2)

Mot-clé

Scarcity (2) Patients (2) Human beings (2) Hypogonadism (2) Patients (2) test (1) protéine (1) association (1) mutation (1) gestion (1) analyse (1) gène (1) famille (1) ADN (1) maladie (1) pièce d'exposition (1) adulte (1) Diagnosis (1) Control (1) Forms (1) Phenotype (1) Genes (1) Syndromes (1) Social groups (1) Signs and symbols (1) Signs and signboards (1) Puberty (1) Medical genetics (1) Management (1) Hypothesis (1)

Documents écrit par A. Nemeth (2) | parle de A. Nemeth (1)

Evaluating CHARGE syndrome in congenital hypogonadotropic hypogonadism patients harboring CHD7 variants.

C. Xu et al.

Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures.

D. Cassatella et al.