CORE
🇺🇦
make metadata, not war
Services
Research
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
Filters
6 research outputs found
Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome.
Author
Beccaria L
Bosio L
+11 more
Carrozzo R
Christian S L
Corrias A
Fois A
Kittikamron K
Ledbetter D H
Livieri C
Pucci L
Rossi E
Simi P
Zuffardi O
Publication venue
Publication date
01/07/1997
Field of study
Get PDF
Elsevier - Publisher Connector
PubMed Central
Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome
Author
BECCARIA L.
BOSIO L.
+11 more
CARROZZO R.
CHRISTIAN S.L.
CORRIAS A.
FOIS A.
KITTIKAMRON K.
LEDBETTER D.H.
LIVIERI C.
PUCCI L.
ROSSI E.
SIMI P.
ZUFFARDI O.
Publication venue
Publication date
Field of study
No full text
Archivio Istituzionale della Ricerca - Università degli Studi di Pavia
Two 22q telomere deletions serendipitously detected by FISH.
Author
C M Lese
Chong S.S.
+21 more
Christian S.L.
D H Ledbetter
Doheny K.F.
Flint J.
Herman G.E.
J C Baker
K Kittikamron
K M Johnston
K S Precht
Narahara K.
Nesslinger N.J.
Ning Y.
P R Huttenlocher
Phelan M.C.
R P Spiro
Romain D.R.
S L Christian
Watt J.L.
Wong A.C.
Yong Y.P.
Zwaigenbaum L.
Publication venue
'BMJ'
Publication date
Field of study
No full text
Crossref
Get PDF
