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2 research outputs found
Phenotypic variability in gap junction syndromic skin disorders: experience from KID and Clouston syndromes’ clinical diagnostics
Author
A Alvarez
A Gilliam
+31 more
A Oshima
AD Irvine
AR Janecke
AY Jan
BA Skinner
EA Zwart-Storm de
FS Burns
GI Hale
GM Essenfelder
J Mazereeuw-Hautier
J Xu
K Natsuga
K Sugiura
L Avshalumova
M Barbareschi
M Cohen-Salmon
M Geel van
MA Steensel van
MA Steensel van
ME Gonzalez
NA Levit
P Calzavara-Pinton
P Gómez-Faiña
PG Hazen
R Bergman
S Arndt
S Yotsumoto
SJ Hassed
SM Elsayed
Z Kibar
ÁF Visinoni
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
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Crossref
Mutations in IMPG1 Cause Vitelliform Macular Dystrophies
Author
Acharya
Acharya
+57 more
Akhavan
Almudena Avila-Fernández
Audrey Sénéchal
Bandah-Rozenfeld
Best
Boon
Boon
Bork
Béatrice Bocquet
Carmen Ayuso García
Catherinot
Christian P. Hamel
Christina Zeitz
Claire-Marie Dhaenens
Coppeto
Delphine Allorge
Deutman
Elfride De Baere
Francesca Simonelli
Frans P.M. Cremers
Gaël Manes
Gehrig
Gilles Labesse
Guylène Le Meur
Gómez-Faiña
Hebrard
Hollyfield
Hélène Dollfus
Isabelle Audo
Isabelle Meunier
Joe G. Hollyfield
José-Alain Sahel
Krämer
Kuehn
Macao
Maeda
Mansergh
Marta Corton
Martyn
Maxime Hebrard
Meunier
Michel Weber
Miyake
Petrukhin
Philippe Brabet
Pérez Alvarez
Robert K. Koenekoop
Saddek Mohand-Said
Salinas Alamán
Sandro Banfi
Seddon
Singh
Sohocki
Susanne Kohl
van den Biesen
van Lith-Verhoeven
Xavier Zanlonghi
Publication venue
'Elsevier BV'
Publication date
Field of study
No full text
Crossref