Carrier screening for inherited haemoglobin disorders among secondary school students and young adults in Latium, Italy-Reference-Cited by-同舟云学术

Carrier screening for inherited haemoglobin disorders among secondary school students and young adults in Latium, Italy

Published:2013-10-27 Issue: Volume: Page:
ISSN:1868-310X
Container-title:Journal of Community Genetics
language:en
Short-container-title:J Community Genet

Author:

Amato Antonio,Cappabianca Maria Pia,Lerone Maria,Colosimo Alessia,Grisanti Paola,Ponzini Donatella,Di Biagio Paola,Perri Maria,Gianni Debora,Rinaldi Silvana,Piscitelli Roberta

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Public Health, Environmental and Occupational Health,Epidemiology

Link

http://link.springer.com/content/pdf/10.1007/s12687-013-0171-z.pdf

Reference21 articles.

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2. Alswaidi FM, O’Brian ZAMSJ, Al-Hamdan NA et al (2012) At-risk marriages after compulsory premarital testing and counseling for β-thalassemia and sickle cell disease in Saudi Arabia. J Genet Couns 21:243–255. doi: 10.1007/s10897-011-9395-4

3. Amato A, Cappabianca MP, Ponzini D et al (2007) Hb L’Aquila [beta 106 (G8) Leu > Val, CTG > GTG]: a novel thalassemic hemoglobin variant. Hemoglobin 31:375–378

4. Amato A, Grisanti P, Lerone M et al (2009) Prevention strategies for severe hemoglobinopathies in endemic and non endemic immigration countries: the Latium example. Prenat Diagn 29:1171–1174. doi: 10.1002/pd.2382

5. Amato A, Lerone P, Grisanti P et al (2011) 35 years of prevention of the Thalassaemia. Ig Sanita Pubbl 67:61–81

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