Hessa S Alsaif

Publication Activity (10 Years)

Years Active: 2020-2021
Publications (10 Years): 3

Top Topics

Intellectual Disability

Acute Kidney Injury

Top Venues

American journal of medical genetics. Part A

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

Publications

Hessa S Alsaif, Ali Alshehri, Raashda A Sulaiman, Hindi Al-Hindi, Francisco J Guzmán-Vega, Stefan T Arold, Fowzan Sami Alkuraya
MYH1 is a candidate gene for recurrent rhabdomyolysis in humans. American journal of medical genetics. Part A 185 (7) (2021)
Hessa S Alsaif, Heba Youssef E L Khashab, Fowzan Sami Alkuraya
Two further cases of polyhydramnios, megalencephaly, and symptomatic epilepsy syndrome, caused by a truncating variant in STRADA. American journal of medical genetics. Part A 185 (2) (2020)
Sateesh Maddirevula, Tawfeg Ben-Omran, Mariam AlMureikhi, Wafaa M Eyaid, Hisham Arabi, Hisham Alkuraya, Abdullah Alfaifi, Abdullah Hamed Alfalah, Hessa S Alsaif, Firdous Abdulwahab, Majid Alfadhel, Fowzan Sami Alkuraya
Further delineation of HIDEA syndrome. American journal of medical genetics. Part A 182 (12) (2020)