S.G. Caraffi

Type de document

Co-auteur

A. Superti-Furga

S. Sassi

M. Pollazzon

L. Garavelli

S. Faccioli

B. Campos-Xavier

M. Valli

S. Unger

E. Soncini

A. Rossi

S. Rosato

M.D. Rocco

A. Percesepe

D. Martorana

M. Marinelli

I. Maini

C. Magnani

I. Ivanovski

T. Grimaldi

S. Giangiobbe

G. Gargano

C. Fusco

D. Frattini

H. Fodstad

G. Comitini

Date

Source

Serveur académique Lausannois (2)

Mot-clé

peau (2) enfant (2) Diagnosis (2) Phenotype (2) Skin (2) Human beings (2) Hand (2) Foot (2) Diagnosis (2) puits (1) tissu (corporel) (1) racine (1) région (1) mutation (1) analyse (1) gène (1) évolution (1) évaluation (1) adulte (1) Dilatation (1) Development (1) Causes (1) Case (1) Forms (1) Cases (1) Abnormalities (1) Genes (1) Dysplasia (1) Variations (1) Thumb (1)

Documents écrit par S.G. Caraffi (2) | parle de S.G. Caraffi (0)

Clinical and Genetic Findings in a Series of Eight Families with Arthrogryposis.

M. Pollazzon et al. (23 déc. 2021)

Severe Peripheral Joint Laxity is a Distinctive Clinical Feature of Spondylodysplastic-Ehlers-Danlos Syndrome (EDS)-B4GALT7 and Spondylodysplastic-EDS-B3GALT6.

S.G. Caraffi et al. (12 oct. 2019)