C. Cavero-Carbonell

发表

M. Posada, Ó. Zurriaga, C. Cavero-Carbonell, 2016, Journal of public health.

C. Cavero-Carbonell, S. Gimeno-Martos, Carlos Pérez-Riera, 2017, Revista espanola de salud publica.

E. Garne, C. Cavero-Carbonell, C. Martos, 2017, Birth defects research.

M. Loane, M. Haeusler, A. Latos-Bieleńska, 2019, Pediatric Research.

M. Loane, M. Gissler, E. Garne, 2022, Orphanet Journal of Rare Diseases.

M. Loane, E. Garne, M. Haeusler, 2015, American journal of medical genetics. Part A.

Ó. Zurriaga, C. Cavero-Carbonell, S. Gimeno-Martos, 2017 .

I. V. van Rooij, M. Loane, A. Latos-Bieleńska, 2020, Birth defects research.

A. Latos-Bieleńska, C. Cavero-Carbonell, A. Materna-Kiryluk, 2018, European journal of medical genetics.

E. Garne, A. Neville, A. Pierini, 2021, Frontiers in Pediatrics.

M. Loane, M. Gissler, E. Garne, 2023, Archives of Disease in Childhood.

Ó. Zurriaga, C. Cavero-Carbonell, S. Gimeno-Martos, 2017, Anales de pediatria.

E. Garne, M. Haeusler, A. Latos-Bieleńska, 2021, Frontiers in Pediatrics.

Ó. Zurriaga, C. Cavero-Carbonell, R. Mas Pons, 2015, Gaceta sanitaria.

Ó. Zurriaga, C. Cavero-Carbonell, F. Corpas-Burgos, 2022, International journal of environmental research and public health.

M. Loane, M. Gissler, E. Garne, 2023, International journal of environmental research and public health.

Ó. Zurriaga, C. Cavero-Carbonell, A. López-Maside, 2016, Anales de pediatria.

M. Loane, M. Gissler, E. Garne, 2022, BMJ Paediatrics Open.

E. Garne, M. Haeusler, A. Neville, 2019, Archives of Disease in Childhood.

E. Garne, M. Haeusler, A. Neville, 2018, European journal of medical genetics.

M. Loane, M. Haeusler, A. Latos-Bieleńska, 2022, American journal of medical genetics. Part A.

F. Bianchi, E. Garne, M. Haeusler, 2019, American journal of medical genetics. Part A.

E. Garne, M. Haeusler, A. Pierini, 2021, Paediatric and perinatal epidemiology.

M. Loane, M. Gissler, E. Garne, 2023, Birth defects research.

Oscar Zurriaga, Juan Rico, Luis Javier Echevarría González de Garibay, 2020, Orphanet Journal of Rare Diseases.