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You searched for: Author/Creator Poulakis, Zeffie

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1. A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort. Issue 3 (24th March 2020)

2. A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort. Issue 1 (14th September 2017)

4. Feasibility and acceptability of targeted salivary cytomegalovirus screening through universal newborn hearing screening. (14th September 2021)

5. Measurement tools for gender identity, gender expression, and gender dysphoria in transgender and gender-diverse children and adolescents: a systematic review. (August 2021)