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Works matching AU Hussein, Ibtessam Ramzi

Results: 2

1

Identification of Extremely Rare Pathogenic CNVs by Array CGH in Saudi Children with Developmental Delay, Congenital Malformations, and Intellectual Disability.

Published in:

Children, 2023, v. 10, n. 4, p. 662, doi. 10.3390/children10040662

By:

Karim, Sajjad;
Hussein, Ibtessam Ramzi;
Schulten, Hans-Juergen;
Alsaedi, Saad;
Mirza, Zeenat;
Al-Qahtani, Mohammed;
Chaudhary, Adeel

Publication type:

Article

2

Molecular Basis of ββ-Thalassemia in the Western Province of Saudi Arabia: Identification of Rare ββ-Thalassemia Mutations.

Published in:

Hemoglobin, 2011, v. 35, n. 4, p. 346, doi. 10.3109/03630269.2011.588508

By:

Abuzenadah, Adel M.;
Hussein, Ibtessam M. Ramzi;
Damanhouri, Ghazi A.;
A-Sayes, Faten M.;
Gari, Mamdouh A.;
Chaudhary, Adeel G.;
Zaher, Galila F.;
Al-Attas, Asma'a;
Al-Qahtani, Mohammad H.

Publication type:

Article