Experiences of predictive testing in young people at risk of Huntington’s disease, familial cardiomyopathy or hereditary breast and ovarian cancer

Original Research

(2012) Rebekah Hamilton   AMERICAN JOURNAL OF NURSING

Genotype inBRCA-associated Breast Cancers

(2012) Funda Meric-Bernstam et al.   Breast Journal

Recommendations for the predictive genetic test in Huntington's disease

(2012) R MacLeod et al.   CLINICAL GENETICS

Life expectancy in hereditary cancer predisposing diseases: an observational study

(2012) Anna Wilding et al.   JOURNAL OF MEDICAL GENETICS

Genetics of Hypertrophic Cardiomyopathy After 20 Years

(2012) Barry J. Maron et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Toward a new understanding of risk perception among young female BRCA1/2 “previvors”.

(2012) Lindsey M. Hoskins et al.   Families Systems & Health

Factors associated with experiences of genetic discrimination among individuals at risk for huntington disease

(2010) Yvonne Bombard et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information

(2009) Gillian Nycum et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genetic testing in asymptomatic minors: recommendations of the European Society of Human Genetics

(2009)   EUROPEAN JOURNAL OF HUMAN GENETICS

The challenge of developmentally appropriate care: predictive genetic testing in young people for familial adenomatous polyposis

(2009) Rony E. Duncan et al.   Familial Cancer

Predictive genetic testing for cardiovascular diseases: Impact on carrier children

(2008) Tineke M. Meulenkamp et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

“You're one of us now”: Young people describe their experiences of predictive genetic testing for Huntington disease (HD) and familial adenomatous polyposis (FAP)

(2008) Rony E. Duncan et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Long-term outcome of presymptomatic testing in Huntington disease

(2008) Marcela Gargiulo et al.   EUROPEAN JOURNAL OF HUMAN GENETICS