1. The use of genealogy databases for risk assessment in genetic health service: a systematic review

   • Vigdis Stefansdottir
   • Oskar Th. Johannsson
   • Jon J. Jonsson

   Review 18 July 2012 Pages: 1 - 7

   

2. Perceptions of genetic research in three rural Appalachian Ohio communities

   • Amy N. Fullenkamp
   • Erin N. Haynes
   • Daniel W. Nebert

   Original Article 05 August 2012 Pages: 9 - 17

   

3. Erratum to: Perceptions of genetic research in three rural Appalachian Ohio communities

   • A. N. Fullenkamp
   • E. N. Haynes
   • L. Meloncon

   Erratum 21 September 2012 Pages: 19 - 19

4. Study of stillbirth and major congenital anomaly among newborns in the high-level natural radiation areas of Kerala, India

   • G. Jaikrishan
   • K. R. Sudheer
   • M. Seshadri

   Original Article 09 August 2012 Pages: 21 - 31

   

5. Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study

   • D. Mohanty
   • R. B. Colah
   • V. Muthuswamy

   Original Article 21 October 2012 Pages: 33 - 42

   

6. Screening for the sickle cell gene in Gujarat, India: a village-based model

   • Jyotish Patel
   • Bharati Patel
   • Graham R. Serjeant

   Original Article 29 September 2012 Pages: 43 - 47

   

7. Examining the family-centred approach to genetic testing and counselling among UK Pakistanis: a community perspective

   • A. Darr
   • N. Small
   • B. Modell

   Original Article 21 October 2012 Pages: 49 - 57

8. Screening criteria: the need to deal with new developments and ethical issues in newborn metabolic screening

   • John Forman
   • Fiona Coyle
   • Michael Legge

   Original Article Open access 07 October 2012 Pages: 59 - 67

9. A study of the practice of individual genetic counsellors and genetic nurses in Europe

   • Heather Skirton
   • Christophe Cordier
   • Anita O’Connor

   Original Article 28 September 2012 Pages: 69 - 75

   

10. The use of a Toolkit for health needs assessment on neural tube defects in Argentina

    • Boris Groisman
    • Rosa Liascovich
    • Gurdeep S. Sagoo

    Original Article 04 October 2012 Pages: 77 - 86

    

11. Prenatal diagnosis and termination of pregnancy: perspectives of South African parents of children with Down syndrome

    • Chantelle Jennifer Scott
    • Merle Futter
    • Ambroise Wonkam

    Original Article 25 October 2012 Pages: 87 - 97

12. Genetics and public health: the experience of a reference center for diagnosis of 22q11.2 deletion in Brazil and suggestions for implementing genetic testing

    • Társis Paiva Vieira
    • Ilária Cristina Sgardioli
    • Vera Lúcia Gil-da-Silva-Lopes

    Original Article 21 October 2012 Pages: 99 - 106

    

13. Experiences of parents with a child with Down syndrome in Pakistan and their views on termination of pregnancy

    • Shenaz Ahmed
    • Louise D. Bryant
    • Yasmin Raashid

    Original Article 23 October 2012 Pages: 107 - 114

14. Conceptions on genetics in a group of college students

    • Patrícia Santana Correia
    • Pedro Vitiello
    • Dafne Dain Gandelman Horovitz

    Original Article 01 November 2012 Pages: 115 - 123

15. The scope of prenatal diagnosis for women at increased risk for aneuploidies: views and preferences of professionals and potential users

    • Antina de Jong
    • Wybo J. Dondorp
    • Guido M. W. R. de Wert

    Original Article 09 November 2012 Pages: 125 - 135

    

16. Inclusion of medical genetics in primary health care: report of a pilot project in Brazil

    • Taiane Alves Vieira
    • Camila Giugliani
    • Roberto Giugliani

    Case Report 25 July 2012 Pages: 137 - 145