J. Pfotenhauer

Type de document

Co-auteur

Z. Xia

S.E. Vallee

M. Summar

P. Stankiewicz

S. Sparks

W.E. Smith

P. Simons

M. Shinawi

C.A. Shaw

T.H. Shaikh

L.G. Shaffer

F. Scaglia

S. Saunders

S. Sampath

J.A. Rosenfeld

A.N. Pursley

K. Platky

A. Patel

S. Parikh

A.R. Paciorkowski

M.J. Noetzel

J.B. Moeschler

L. Medne

T.L. McGregor

D. Martinet

A.S. Martin

S. Madan-Khetarpal

C.M. Lovell

B. Lee

J.L. Kussmann

S. Kulkarni

S.H. Kang

P. Irwin

J. Hoover

R. Hamid

D.K. Grange

J.L. Gorski

K. Golden-Grant

D.B. Flannery

F. Fellmann

A.V. Dharmadhikari

V.P. Dalzell

M.L. Cooper

S.W. Cheung

C.G. Bonnemann

S.S. Bhatt

G.A. Bellus

J.S. Beckmann

V.C. Banks

B.C. Ballif

C.A. Bacino

A. Asamoah

Date

Source

Serveur académique Lausannois (1)

Mot-clé

nourisson (1) sommeil (1) cartographie (cartes) (1) analyse (1) variation génétique (1) gène (1) évaluation (1) ADN (1) pièce d'exposition (1) enfant (1) Deletion (1) Cases (1) Abnormalities (1) In situ hybridization (1) Acetyltransferases (1) Variations (1) Transportation (1) Sleep (1) Patients (1) Parents (1) Nystagmus (1) Human beings (1) Identity (Philosophical concept) (1) Growth (1) Fluorescence (1) Evaluation (1) Epilepsy (1) DNA (1) Deglutition disorders (1) Constipation (1)

Documents écrit par J. Pfotenhauer (1) | parle de J. Pfotenhauer (0)

Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.

P. Stankiewicz et al. (2012)