Rasha Moheb Elhossini (Rasha M Elhossini)

Publication Activity (10 Years)

Years Active: 2022-2023
Publications (10 Years): 6

Top Topics

End Stage Renal Disease

Ejection Fraction

Patient Reported Outcomes

Top Venues

American journal of medical genetics. Part A

Congenital anomalies

Molecular genetics and genomics : MGG

This page only lists publications with an associated author ORCID identifier.

Publications

Rasha Moheb Elhossini, Inas S M Sayed, Usama Saad Hellal, Sarah A M Mahmoud, Mona S Aglan, Nehal F Hassib, Mohamed S Abdel-Hamid
A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management. American journal of medical genetics. Part A (2023)
Ghada A Otaify, Rasha Moheb Elhossini, Sherif F Abdel-Ghafar, Inas S M Sayed, Ghada M H Abdel-Salam, Mona S Aglan, Mohamed S Abdel-Hamid
CHST3-related skeletal dysplasia in 14 patients: Identification of 8 novel variants and further expansion of the phenotypic spectrum. American journal of medical genetics. Part A (2023)
Rasha Moheb Elhossini, Hasnaa M Elbendary, Karima Rafat, Raghda M Ghorab, Mohamed S Abdel-Hamid
Spondyloenchondrodysplasia in five new patients: identification of three novel ACP5 variants with variable neurological presentations. Molecular genetics and genomics : MGG (2023)
Ghada A Otaify, Mohamed S Abdel-Hamid, Nehal F Hassib, Rasha Moheb Elhossini, Sherif F Abdel-Ghafar, Mona S Aglan
Bruck syndrome in 13 new patients: Identification of five novel FKBP10 and PLOD2 variants and further expansion of the phenotypic spectrum. American journal of medical genetics. Part A 188 (6) (2022)
Rasha Moheb Elhossini, Mohamed S Abdel-Hamid, Engy Ashaat, Ghada A Otaify, Heba Dawoud, Khalid Elshimy, Mona El Ruby, Mona Aglan
Two new patients with focal dermal hypoplasia: A novel PORCN variant and insights on the diagnostic considerations. Congenital anomalies 62 (2) (2022)
Rasha Moheb Elhossini, Hoda Abdalla Ahmed, Ghada A Otaify, Raghda M Ghorab, Khalda Sayed Amr, Mona Aglan
A novel variant in GNPNAT1 gene causing a spondylo-epi-metaphyseal dysplasia resembling PGM3-Desbuquois like dysplasia. American journal of medical genetics. Part A 188 (10) (2022)