C. Inglehearn

Type de document

Co-auteur

P.M. Yamaguti

S.B. Walsh

M. Vikkula

A. Verloes

R. J. Unwin

H.C. Stanescu

G. Spartà

R. Shore

M. Schmittbuhl

E. Schlatter

S.J. Scheinman

C. Sandmann

H.P. Safatle

D. Ruehmann

G Roussey

S.L. Robinette

A. Rauch

M. Quentric

S. Povey

J. Poulter

A. Picard

V. Patel

D. Parry

S. Pajarola

D. Ozdemir-Ozenen

J.K. Nicholson

U. Neugebauer

A. Mighell

A.J. Medlar

D.A. McCredie

H. Martelli-Júnior

C. Logan

C. Le Caignec

V Laugel

C.B. Langman

C. Laing

T. Koike

E. Klootwijk

R. Kleta

H. Kitagawa

C Johnson

G. Jaureguiberry

N. Issler

B. Isidor

M. Huckert

A.J. Howie

P. Houillier

N. Himmerkus

T.C. Hart

P.S. Hart

J. Guiol

S. Gruessel

E. Ginglinger

W.A. Gahl

M.L. Figueres

P.E. dos Santos Netos

M. De la Dure-Molla

A. Coulomb

R.D. Coletta

F. Clauss

D. Bockenhauer

A. Bloch-Zupan

M. Bleich

A Berdal

D. Bartholdi

I. Bailleul-Forestier

A. Asselin

S. Al-Bahlani

M.C. Addor

A.C. Acevedo

Date

Source

Serveur académique Lausannois (1)

Mot-clé

spectacle (1) association (1) mutation (1) ion (1) analyse (1) gène (1) maladie (1) enfant (1) adulte (1) calcium (1) jeune (1) Defects (1) Causes (1) Causative (1) Methods (1) Teeth--Eruption (1) Genes (1) Kidneys--Calcification (1) Will (1) Social groups (1) Patients (1) Human beings (1) Kidneys--Calculi (1) Homeostasis (1) Gingival hyperplasia (1) Families--Health and hygiene (1) Families (1) Dental enamel (1) Defects (1) Consanguinity (1)

Documents écrit par C. Inglehearn (1) | parle de C. Inglehearn (0)

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations.

G. Jaureguiberry et al. (2012)