Mary Petrou
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
The parental perspective of thalassaemia in Bangladesh: lack of knowledge, regret, and barriers.
Journal: Orphanet journal of rare diseases
Published: May 24, 2021
Lack of knowledge and misperceptions about thalassaemia among college students in Bangladesh: a cross-sectional baseline study.
Journal: Orphanet journal of rare diseases
Published: November 28, 2019
A method for noninvasive prenatal diagnosis of monogenic autosomal recessive disorders.
Journal: Blood
Published: August 25, 2019
Rare single gene disorders: estimating baseline prevalence and outcomes worldwide.
Journal: Journal of community genetics
Published: March 21, 2018
Preferences for prenatal diagnosis of sickle-cell disorder: A discrete choice experiment comparing potential service users and health-care providers.
Journal: Health expectations : an international journal of public participation in health care and health policy
Published: April 01, 2017
EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.
Journal: European journal of human genetics : EJHG
Published: March 13, 2015
EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.
Journal: European journal of human genetics : EJHG
Published: February 22, 2014
Prenatal diagnosis for thalassaemia in Egypt: what changed parents' attitude?
Journal: Prenatal diagnosis
Published: June 14, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026