Latest papers

Policy implications of early onset breast cancer among Mexican-origin women.

[The influence of parents personality and DRD4 and 5HTT genes polymorphisms on predisposition to alcohol dependence in their sons].

Understanding ethnic/racial health disparities in youth and families in the US.

HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes.

Serving and supporting young children with a dual diagnosis of hearing loss and autism: the stories of four families.

Spinocerebellar ataxia type 10.

A novel EIF2AK3 mutation leading to Wolcott-Rallison syndrome in a Chinese child.

Spinocerebellar ataxia type 28.

Spinocerebellar ataxia type 12.

Spinocerebellar ataxia type 7.

Spinocerebellar ataxia type 11.

Evangelicalism and the early vegetarian movement in Britain c.1847–1860.

Family supports and resources for parents of children who are deaf or hard of hearing.

Clinical and genetic features of spinocerebellar ataxia type 8.

The Swedish Multi-generation Register.

Personal stories: voices of latino youth health advocates in a diabetes prevention initiative.

The rise and fall of domestic chemistry in higher education in England during the early 20th century.

The use of TeleMedicine in the treatment of paediatric obesity: feasibility and acceptability.

Spinocerebellar ataxia type 5.

Depressive symptoms evaluated by the Calgary Depression Scale for Schizophrenia (CDSS): genetic vulnerability and sex effects.