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Pregled bibliografske jedinice broj: 674934

Advancing rare disease research: the use of network of congenital anomaly registries in the study of rare genetic syndromes

Odak, Ljubica; Barišić, Ingeborg; Loane, M; Garne, E; Wellesley, D; Calzolari, E; Dolk, H; EUROCAT Working Group
Advancing rare disease research: the use of network of congenital anomaly registries in the study of rare genetic syndromes // Book of abstracts of 12th European Symposium on Congenital Anomalies
Zagreb: European Surveillance of Congenital Anomalies Association, 2013. str. 89-89 (poster, međunarodna recenzija, sažetak, ostalo)

CROSBI ID: 674934 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Advancing rare disease research: the use of network of congenital anomaly registries in the study of rare genetic syndromes

Autori
Odak, Ljubica ; Barišić, Ingeborg ; Loane, M ; Garne, E ; Wellesley, D ; Calzolari, E ; Dolk, H ; EUROCAT Working Group

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo

Izvornik
Book of abstracts of 12th European Symposium on Congenital Anomalies / - Zagreb : European Surveillance of Congenital Anomalies Association, 2013, 89-89

Skup
12th European Symposium on Congenital Anomalies

Mjesto i datum
Zagreb, Hrvatska, 14.06.2013

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
rare disease; research

Sažetak
Advancing rare disease research: the use of network of congenital anomaly registries in the study of rare genetic syndromes

Izvorni jezik
Engleski



POVEZANOST RADA

Projekti:
072-1083107-0365 - Istraživanje epidemiologijskih i genetičkih osnova prirođenih mana (Barišić, Ingeborg, MZOS ) ( CroRIS)

Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta

Profili:

Avatar Url Ingeborg Barišić (autor)

Avatar Url Ljubica Boban (autor)

Citiraj ovu publikaciju:

Odak, Ljubica; Barišić, Ingeborg; Loane, M; Garne, E; Wellesley, D; Calzolari, E; Dolk, H; EUROCAT Working Group
Advancing rare disease research: the use of network of congenital anomaly registries in the study of rare genetic syndromes // Book of abstracts of 12th European Symposium on Congenital Anomalies
Zagreb: European Surveillance of Congenital Anomalies Association, 2013. str. 89-89 (poster, međunarodna recenzija, sažetak, ostalo)
Odak, L., Barišić, I., Loane, M., Garne, E., Wellesley, D., Calzolari, E., Dolk, H. & EUROCAT Working Group (2013) Advancing rare disease research: the use of network of congenital anomaly registries in the study of rare genetic syndromes. U: Book of abstracts of 12th European Symposium on Congenital Anomalies.
@article{article, author = {Odak, Ljubica and Bari\v{s}i\'{c}, Ingeborg and Loane, M and Garne, E and Wellesley, D and Calzolari, E and Dolk, H}, year = {2013}, pages = {89-89}, keywords = {rare disease, research}, title = {Advancing rare disease research: the use of network of congenital anomaly registries in the study of rare genetic syndromes}, keyword = {rare disease, research}, publisher = {European Surveillance of Congenital Anomalies Association}, publisherplace = {Zagreb, Hrvatska} }
@article{article, author = {Odak, Ljubica and Bari\v{s}i\'{c}, Ingeborg and Loane, M and Garne, E and Wellesley, D and Calzolari, E and Dolk, H}, year = {2013}, pages = {89-89}, keywords = {rare disease, research}, title = {Advancing rare disease research: the use of network of congenital anomaly registries in the study of rare genetic syndromes}, keyword = {rare disease, research}, publisher = {European Surveillance of Congenital Anomalies Association}, publisherplace = {Zagreb, Hrvatska} }

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