Search Results - "Al-Rashdi, Samiya"

Reanalysis of exome sequencing data of intellectual disability samples: Yields and benefits.

Authors: Al‐Nabhani, Maryam Al‐Rashdi, Samiya Al‐Murshedi, Fathiya et al.

Source: Clinical Genetics. Dec2018, Vol. 94 Issue 6, p495-501. 7p. 1 Diagram, 2 Charts.

Single-centre comparison of non-familial, familial and monogenic lupus.

Authors: Alshekaili, Jalila Lawati, Batool S H Al Althuhli, Zahran et al.

Source: Rheumatology. Oct2025, Vol. 64 Issue 10, p5388-5395. 8p.

The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families.

Authors: Al-Kasbi, Ghalia Al-Murshedi, Fathiya Al-Kindi, Adila et al.

Source: Scientific Reports. 11/7/2022, Vol. 12 Issue 1, p1-12. 12p.

Shohat type-spondyloepimetaphyseal dysplasia: Further phenotypic delineation.

Authors: Otaify, Ghada A. Al Baluki, Wafa Al-Rashdi, Samiya et al.

Source: European Journal of Medical Genetics. Dec2022, Vol. 65 Issue 12, pN.PAG-N.PAG. 1p.

Biallelic mutations in AP3D1 cause Hermansky-Pudlak syndrome type 10 associated with immunodeficiency and seizure disorder.

Authors: Mohammed, Mohammed Al-Hashmi, Nadia Al-Rashdi, Samiya et al.

Source: European Journal of Medical Genetics. Nov2019, Vol. 62 Issue 11, pN.PAG-N.PAG. 1p.