Heba Hassan
6PUBLICATIONS
5CO-AUTHORS
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Publications (6)
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|Feb 27, 2026
Novel Homozygous DLX5 and WNT10B Variants Expand the Genetic and Phenotypic Spectrum of Autosomal Recessive Split-Hand/Foot Malformations (SHFM1D and SHFM6).Heba A Hassan, Asmaa M Esmail, Mervat Elbelbesy
|Feb 16, 2026
Clinical Utility of Genetic Diagnosis in Drug-Resistant Epilepsy: Refining Classification and Guiding Therapy in an Egyptian Cohort.Wessam E Sharaf-Eldin, Nirmeen A Kishk, Noura R Eissa
|Mar 25, 2024
Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II.Heba Amin Hassan, Inas Mazen, Aya Elaidy
|Mar 20, 2021
Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development.Inas Mazen, Mona Mekkawy, Alaa Kamel
|Jul 16, 2020
Novel mutations of the LHCGR gene in two families with 46,XY DSD causing Leydig cell hypoplasia I.Heba Amin Hassan, M L Essawi, M K Mekkawy
|Jul 03, 2020
Assessment of the most common CYP21A2 point mutations in a cohort of congenital adrenal hyperplasia patients from Egypt.Mona Essawi, Inas Mazen, Lubna Fawaz
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