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4 research outputs found
KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome
Author
Amaya Bengoa-Alonso
Aranzazu PĂ©rez-Juana-del-Casal
+5Â more
Beatriz Nieva-Echebarria
Blanca Hernández-Charro
Carlos Romero-Ibarra
MarĂa Antonia Ramos-Arroyo
MarĂa Moreno-Igoa
Publication venue
Springer Nature
Publication date
01/01/2015
Field of study
Get PDF
Springer - Publisher Connector
KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome
Author
Amaya Bengoa-Alonso
Aranzazu PĂ©rez-Juana-del-Casal
+26Â more
Beatriz Nieva-Echebarria
Blanca Hernández-Charro
C Dubourg
C Shaw-Smith
Carlos Romero-Ibarra
CD Wray
D Ren
DA Koolen
DA Koolen
DA Koolen
EB Wright
G Terrone
GM Cooper
H Dornelles-Wawruk
H Solomon
JP Rouault
M Nadal
M Zollino
MarĂa Antonia Ramos-Arroyo
MarĂa Moreno-Igoa
R Bachmann-Gagescu
SM Gribble
TY Tan
WE Tidyman
X Li
Y Cai
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
Full text link
Crossref
El polimorfismo ACT/AA podrĂa duplicar el riesgo de enfermedad de Alzheimer asociado al alelo APOE*ε4
Author
Alberto Valiente
Blanca Hernández-Charro
+4Â more
JosĂ© MarĂa Manubens
MarĂa Antonia Ramos-Arroyo
MarĂa Dolores Villar
Sira Moreno
Publication venue
'Elsevier BV'
Publication date
Field of study
No full text
Crossref
El polimorfismo ACT/AA podria duplicar el riesgo de enfermedad de Alzheimer asociado al alelo APOE*ε4
Author
Abraham
Alberto Valiente
+32Â more
Alvarez
Barger
Blanca Hernández-Charro
Blesa
Combarros
Dickson
Egensperger
Ezquerra
Haines
Hull
Itabashi
JosĂ© MarĂa Manubens
Kamboh
Kelsey
Kim
Lahoz
MarĂa Antonia Ramos-Arroyo
MarĂa Dolores Villar
McGeer
McKhann
Miller
Muller
Muramatsu
Nacmias
Potter
Prince
Sira Moreno
Strittmatter
Tang
Wang
Wenham
Yoshiiwa
Publication venue
'Elsevier BV'
Publication date
Field of study
No full text
Crossref