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Balkan Journal of Medical Genetics
Volume 24 (2021): Numero 1 (June 2021)
Accesso libero
Association of
NFKB1
,
NKX2-5
,
GATA4
and
RANKL
gene polymorphisms with sporadic congenital heart disease in Greek patients
L Aidinidou
L Aidinidou
,
A Chatzikyriakidou
A Chatzikyriakidou
,
A Giannopoulos
A Giannopoulos
,
V Karpa
V Karpa
,
I Tzimou
I Tzimou
,
E Aidinidou
E Aidinidou
e
L Fidani
L Fidani
| 27 lug 2021
Balkan Journal of Medical Genetics
Volume 24 (2021): Numero 1 (June 2021)
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CONDIVIDI
Article Category:
Original Article
Pubblicato online:
27 lug 2021
Pagine:
15 - 20
DOI:
https://doi.org/10.2478/bjmg-2021-0014
Parole chiave
Congenital heart disease (CHD)
,
(–94ins/delATTG)
,
© 2021 Aidinidou L, Chatzikyriakidou A, Giannopoulos A, Karpa V, Tzimou I, Aidinidou E, Fidani L, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
L Aidinidou
Department of Medical Biology-Genetics, Medical School, Aristotle University of Thessaloniki
Thessaloniki, Greece
A Chatzikyriakidou
Department of Medical Biology-Genetics, Medical School, Aristotle University of Thessaloniki
Thessaloniki, Greece
A Giannopoulos
Second Department of Pediatrics, Pediatric Cardiology Clinic, AHEPA University Hospital, Aristotle University of Thessaloniki
Thessaloniki, Greece
V Karpa
Department of Medical Biology-Genetics, Medical School, Aristotle University of Thessaloniki
Thessaloniki, Greece
I Tzimou
Second Department of Pediatrics, Pediatric Cardiology Clinic, AHEPA University Hospital, Aristotle University of Thessaloniki
Thessaloniki, Greece
E Aidinidou
Department of Microbiology, Health Center of Prinos, Thassos Island
Macedonia, Greece
L Fidani
Department of Medical Biology-Genetics, Medical School, Aristotle University of Thessaloniki
Thessaloniki, Greece