@ARTICLE{
author={Pasic Srdjan S,Vujic Dragana S,Veljkovic Dobrila K,Slavkovic Bojana,Mostarica-Stojkovic Marija B,Minic Predrag B,Minic Aleksandra,Ristic Goran G,Giliani Silvia,Villa Anna,Sobacchi Cristina,Lilic Desa,Abinun Mario},
year={2014},
title={Severe Combined Immunodeficiency in Serbia and Montenegro Between Years 1986 and 2010: A Single-Center Experience},
journal={JOURNAL OF CLINICAL IMMUNOLOGY},
volume={34},
number={3},
pages={304-308},
document_type={Article},
} 

@ARTICLE{
author={Frattini A,Pangrazio A,Susani L,Sobacchi Cristina,Mirolo M,Abinun Mario,Andolina M,Flanagan A,Horwitz EM,Mihci E,Notarangelo LD,Ramenghi U,Teti A,van Hove JLK,Vujic Dragana S,Young T,Albertini A,Orchard PJ,Vezzoni P,Villa A},
year={2003},
title={Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis},
journal={JOURNAL OF BONE AND MINERAL RESEARCH},
volume={18},
number={10},
pages={1740-1747},
document_type={Article},
} 

@ARTICLE{
author={Sobacchi Cristina,Frattini A,Orchard PJ,Porras O,Tezcan I,Andolina M,Babul-Hirji R,Baric I,Canham N,Chitayat D,Dupuis-Girod S,Ellis I,Etzioni A,Fasth A,Fisher A,Gerritsen B,Gulino V,Horwitz EM,Klamroth V,Lanino E,Mirolo M,Musio A,Matthijs G,Nonomaya S,Notarangelo LD,Ochs HD,Furga AS,Valiaho J,van Hove JLK,Vihinen M,Vujic Dragana S,Vezzoni P,Villa A},
year={2001},
title={The mutational spectrum of human malignant autosomal recessive osteopetrosis},
journal={HUMAN MOLECULAR GENETICS},
volume={10},
number={17},
pages={1767-1773},
document_type={Article},
} 

@ARTICLE{
author={Villa A,Sobacchi Cristina,Notarangelo LD,Bozzi F,Abinun Mario,Abrahamsen TG,Arkwright PD,Baniyash M,Brooks EG,Conley ME,Cortes P,Duse M,Fasth A,Filipovic Aleksandra M,Infante AJ,Jones A,Mazzolari E,Muller SM,Pasic Srdjan S,Rechavi G,Sacco MG,Santagata S,Schroeder ML,Seger R,Strina D,Ugazio A,Valiaho J,Vihinen M,Vogler LB,Ochs H,Vezzoni P,Friedrich W,Schwarz K},
year={2001},
title={V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations},
journal={BLOOD},
volume={97},
number={1},
pages={81-88},
document_type={Article},
} 

@ARTICLE{
author={Santagata S,Gomez CA,Sobacchi Cristina,Bozzi F,Abinun Mario,Pasic Srdjan S,Cortes P,Vezzoni P,Villa A},
year={2000},
title={N-terminal RAG1 frameshift mutations in Omenn's syndrome: Internal methionine usage leads to partial V(D)J recombination activity and reveals a fundamental role in vivo for the N-terminal domains},
journal={PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA},
volume={97},
number={26},
pages={14572-14577},
document_type={Article},
} 

@ARTICLE{
author={Villa A,Bozzi F,Sobacchi Cristina,Strina D,Fasth A,Pasic Srdjan S,Notarangelo LD,Vezzoni P},
year={2000},
title={Prenatal diagnosis of RAG-deficient Omenn syndrome},
journal={PRENATAL DIAGNOSIS},
volume={20},
number={1},
pages={56-59},
document_type={Article},
}