檢索結果 - Fayez, Alaaeldin

Variable predicted pathogenic mechanisms for novel MECP2 variants in RTT patients 由 Sharaf-Eldin, Wessam E., Issa, Mahmoud Y., Zaki, Maha S., Kilany, Ayman, Fayez, Alaaeldin G.

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A Novel Loss-of-Sclerostin Function Mutation in a First Egyptian Family with Sclerosteosis 由 Fayez, Alaaeldin, Aglan, Mona, Esmaiel, Nora, El Zanaty, Taher, Abdel Kader, Mohamed, El Ruby, Mona

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Independent of DAZL-T54A variant and AZF microdeletion in a sample of Egyptian patients with idiopathic non-obstructed azoospermia 由 Shafae, Mohammed M El, Sabry, Jehan H, Behiry, Eman G, Sabry, Hanan H, Salim, Mona A, Fayez, Alaaeldin G

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An infertile azoospermic male with 45,X karyotype and a unique complex (Y;14); (Y;22) translocation: cytogenetic and molecular characterization 由 Mekkawy, Mona K., El Guindi, Ahmed M., Mazen, Inas M., Fayez, Alaaeldin G., Mohamed, Amal M., Kamel, Alaa K.

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Dynamic disequilibrium-based pathogenicity model in mutated pyrin’s B30.2 domain—Casp1/p20 complex 由 Fayez, Alaaeldin G., Eldeen, Ghada Nour, Zarouk, Waheba A., Hamed, Khaled, Ramadan, Abeer, Foda, Bardees M., Kobesiy, Maha M., Zekrie, Mai E., Lotfy, Randa S., Sokkar, Mona F., El-Bassyouni, Hala T.

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DALIA- a comprehensive resource of Disease Alleles in Arab population 由 Vatsyayan, Aastha, Sharma, Parul, Gupta, Shrey, Sandhu, Sumiti, Venu, Seetha Lakshmi, Sharma, Vandana, Badaoui, Bouabid, Azedine, Kaidi, Youssef, Serti, Rajab, Anna, Fayez, Alaaeldin, Madinur, Seema, Ranawat, Anop, Pandhare, Kavita, Ramachandran, Srinivasan, Sivasubbu, Sridhar, Scaria, Vinod

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