Ethnic disparity in 21-hydroxylase gene mutations identified in Pakistani congenital adrenal hyperplasia patients

Overview of attention for article published in BMC Endocrine Disorders, February 2011

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dimensions_citation: 18 Dimensions

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So far, Dimensions has found 18 publications that cite this research output.

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Inborn errors of metabolism: Historical perspectives to contemporary management

Article in Clinica Chimica Acta (July 2024)

Cross-Cultural Disparities in Psychosocial Research with Individuals with Classical Congenital Adrenal Hyperplasia: A Scoping Review

Article in Hormone Research in Paediatrics (August 2023)

Cost-effective genotyping for classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) in resource-poor settings: multiplex ligation probe amplification (MLPA) with/without sequential next-generation sequencing (NGS)

Article in Hormones (March 2023)

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