CORE
CO
nnecting
RE
positories
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
Research partnership
About
About
About us
Our mission
Team
Blog
FAQs
Contact us
Community governance
Governance
Advisory Board
Board of supporters
Research network
Innovations
Our research
Labs
Filters
5 research outputs found
Carrier screening for ?- and ?-thalassemia in pregnancy: the results of an 11-year prospective program in Guangzhou Maternal and Neonatal hospital
Author
Alwan
Cai
+33 more
Cao
Cao
de Silva
Fucharoen
Ghanei
Greengross
Guidelines for investigation of the alpha and beta thalassaemia traits
Jaovisidha
Karimi
Lam
Lam
Liao
Lorey
Modell
National Hemoglobinopathy Cooperative Study Group
Perera
Saxena
Tongsong
WHO Hereditary Disease Programme
WHO Human Genetics Programme
Wu
Wu
Xiao
Xu
Xu
Xu
Xu
Xu
Zeng
Zeng
Zhang
Zhang
Zhang
Publication venue
'Wiley'
Publication date
01/01/2005
Field of study
No full text
Crossref
Autosomal dominant polycystic kidney disease in the 1980's
Author
Alexander
Bear
+21 more
Brackenridge
Breuning
Chappie
Dalgaard
Dalgaard
Higgs
Hossack
Jarman
Kimberling
McKusick
McKusick
Mooney
Ncrby
Nerby
Norby
Reeders
Reeders
Reeders
Reeders
Report of the Task Group on WHO Human Genetics Programme Health for All by the Year 2000
Romeo
Publication venue
'Wiley'
Publication date
Field of study
No full text
Crossref
An Overview of the Homozygous Cystic Fibrosis Transmembrane Conductance Regulator Mutation c.3700 A>G (p.Ile1234Val) in Qatar
Author
A Abdul Wahab
A Abdul Wahab
+34 more
A Abdul Wahab
A Abdul-Wahab
A AbdulWahab
A AbdulWahab
A AbdulWahab
A Quint
AA Wahab
AA Wahab
AA Wahab
AA Wahab
B Kerem
CFTR Science
Duaa Al-Sadeq
EA el-Harith
Gitte Berkers
H Abdel Rahman
H Banjar
HA Eskandarani
J Zielenski
Jacquelien Noordhoek
JL Bobadilla
JM Rommens
JR Riordan
JS Elborn
K Dawson
K De Boeck
M Claustres
M Kambouris
M Marangi
O Reish
SS Elshafie
SV Molinski
UW Fass
WHO Human Genetics Programme
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
No full text
Crossref
Prevalence of inadequate intake of folate after mandatory fortification: results from the first National Dietary Survey in Brazil
Author
A Moshfegh
AD Smith
+48 more
AE Czeizel
AL Carriquiry
AM Cordero
AM Souza
B de Benoist
Brasil. Ministério da Saúde
Cecília Zanin Palchetti
CG Victora
CM Pfeiffer
CZ Palchetti
DC Malta
Dirce Maria Lobo Marchioni
DML Marchioni
EA Yetley
EL Korn
Eliseu Verly
Food and Drug Administration
Food and Drug Administration
G Sedgh
GM Shaw
HC Hamner
Institute of Medicine National Academy of Sciences
International Clearinghouse for Birth Defects Monitoring Systems. International Centre for Birth Defects WHO Human Genetics Programme & European Registration of Congenital Anomalies
J Al-Tahan
J Rosenthal
J Steluti
J Steluti
JA Tooze
JB Mason
JI Rader
Josiane Steluti
JY Park
KH Brunacio
LMP Santos
MC Morris
MJ Khoury
MM Werler
MR Vitolo
MS Field
MS Morris
No authors listed
Q Yang
RL Bailey
Rosangela A. Pereira
Rosely Sichieri
S Hirsch
T Tamura
YA Shakur
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
No full text
Crossref
The panorama of familial hypercholesterolemia in Latin America: a systematic review
Author
Aguilar-Salinas
Aguilar-Salinas
+118 more
Ahmad
Ahualli
Alberto
Alejandra Vazquez-Cárdenas
Alexandro J. Martagón
Alonso
Araujo
Araujo
Arteaga
Ballesteros
Barros
Bednarska-Makaruk
Bell
Benn
Bertolini
Besseling
Bruckert
Burgos
Cabrera
Canizales-Quinteros
Carlos A. Aguilar-Salinas
Cefalù
Cenarro
Cohen
de Ferranti
Defesche
deGoma
DeMott
Dos Santos
Esperon
Esperón
Farnier
Farzadfar
Figueiredo
Freire
Gencera
Genest
Gidding
Goldberg
Goldstein
González
Gómez-Pérez
Harada-Shiba
Haralambos
Haralambos
Hobbs
Homedes
Huijgen
Ito
Jacobson
Jannes
Jiménez-Corona
Khera
Kotze
Krogh
Leitersdorf
Lotufo
Mabuchi
Magaña Torres
Malta
Martinez
María Teresa Tusié-Luna
Mata
Mata
Medeiros
Merchán
Moher
Mohrschladt
Mortensen
Mundal
Mundal
Najam
Ned
Neil
Nherera
Nordestgaard
O'Brien
Palacios
Pereira
Pereira
Piepoli
Pijlman
Pr#xFCss-#xDCst#xFCn
Rafael Zubirán
Robles-Osorio
Robles-Osorio
Rocha
Roopa Mehta
Rynkiewicz
Salazar
Santos
Santos
Santos
Santos
Santos
Sharifi
Singh
Stoll
Thiart
Thompson
Umans-Eckenhausen
Vaca
Vallejo-Vaz
van de Kerkhof
Versmissen
Vogt
Vuorio
Watts
Watts
Weng
WHO Human Genetics Programme
Williams
Wong
Yamamoto
Yayoi Segura-Kato
Yu
Yu
Ågård
Publication venue
'American Society for Biochemistry & Molecular Biology (ASBMB)'
Publication date
Field of study
No full text
Crossref