CORE
🇺🇦
make metadata, not war
Services
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
1 research outputs found
Array comparative genomic hybridization and genomic sequencing in the diagnostics of the causes of congenital anomalies
Author
A Bhattacharjee
A Hoischen
+86 more
A Itsara
A Kallioniemi
A Latos-Bieleńska
A Narravula
A Vetro
A Weise
AM Slavotinek
AM Slavotinek
B Rabbani
BG Ng
BG Ng
BM Helm
C Gilissen
C-K Cheon
CB Cargile
CMR Campos
D Grozeva
D Johnson
D Schanze
DG MacArthur
DL Bodian
DR Bertola
DT Miller
DY Hwang
E Calzolari
E Calzolari
E Giorgio
E Goldmuntz
E Roessler
E Schaefer
EM Bonachea
F Conte
F Erdogan
FS Jehee
G Caruana
G Kellogg
GP Jarvik
H Watkins
HC Mefford
HL Rehm
IT Peltekova
J Casey
J Geng
JE Ming
JH Tjio
JR Vermeesch
K Rojnueangnit
K Szczałuba
K Szczałuba
K Tammimies
KJ Carss
KM Bujakowska
KW Gripp
KW Gripp
LD Kotan
M Grunert
M Margulies
M Moreno-Igoa
M Simioni
MC Hannibal
MN Bainbridge
MS Raam
N Bögershausen
N Dargis
N Miyake
NL Couser
P Bütikofer
PD Brady
PL Crotwell
Polish Registry of Congenital Malformations Team
Q Xi
R Soemedi
RCM Hennekam
S Ayub
S Girirajan
S Hayashi
S Weber
SB Ng
SC Greenway
SR Twigg
TD Gelehrter
TF Beck
TJ Pugh
W Maarse
X-Y Lu
Z Stark
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
No full text
Crossref