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Author/Creator Abubaker, Rayan

1. Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencing. (3rd February 2022)

Authors:
Yahia, Ashraf; Ayed, Ikhlas Ben; Hamed, Ahlam A.; Mohammed, Inaam N.; Elseed, Maha A.; Bakhiet, Aisha M.; Guillot‐Noel, Lena; Abozar, Fatima; Adil, Rawaa; Emad, Sara; Abubaker, Rayan; Musallam, Mhammed Alhassan; Eltazi, Isra Z. M.; Omer, Zulfa; Maaroof, Omer M.; Soussi, Amal; Bouzid, Amal; Kmiha,...
Journal:
Annals of human genetics
Issue:
Volume 86:Number 4(2022)
Page Start:
181
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Methylation of alpha-synuclein in a Sudanese cohort. (August 2022)

Authors:
Bakhit, Yousuf; Schmitt, Ina; Hamed, Ahlam; Ibrahim, Etedal Ahmed A.; Mohamed, Inaam N.; El-Sadig, Sarah M.; Elseed, Maha A.; Alebeed, Mohamed A.; Shaheen, Mutaz T.; Ibrahim, Mohamed O.; Elhassan, Ali A.; Eltom, Khalid; Ali, Hiba A.; Ibrahim, Yousuf A.; Almak, Murad E.; Abubaker, Rayan; Ahmed, Mo...
Journal:
Parkinsonism & related disorders
Issue:
Volume 101(2022)
Page Start:
6
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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