Rasha Moheb Elhossini
7PUBLICATIONS
6CO-AUTHORS
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Publications (7)
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|Mar 22, 2025
Deciphering the phenotypic spectrum associated with MIA3-related odontochondrodysplasia.Mohamed S Abdel-Hamid, Rasha M Elhossini, Sherif F Abdel-Ghafar
|Sep 26, 2023
A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management.Rasha M Elhossini, Inas M Sayed, Usama Saad Hellal
|May 15, 2023
CHST3-related skeletal dysplasia in 14 patients: Identification of 8 novel variants and further expansion of the phenotypic spectrum.Ghada A Otaify, Rasha M Elhossini, Sherif F Abdel-Ghafar
|Apr 03, 2023
Spondyloenchondrodysplasia in five new patients: identification of three novel ACP5 variants with variable neurological presentations.Rasha M Elhossini, Hasnaa M Elbendary, Karima Rafat
|Sep 13, 2022
A novel variant in GNPNAT1 gene causing a spondylo-epi-metaphyseal dysplasia resembling PGM3-Desbuquois like dysplasia.Rasha Moheb Elhossini, Hoda Abdalla Ahmed, Ghada Otaify
|Mar 12, 2022
Bruck syndrome in 13 new patients: Identification of five novel FKBP10 and PLOD2 variants and further expansion of the phenotypic spectrum.Ghada A Otaify, Mohamed S Abdel-Hamid, Nehal F Hassib
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