Rezultati - Althagafi, Azza

Predicting candidate genes from phenotypes, functions and anatomical site of expression od Chen, Jun, Althagafi, Azza, Hoehndorf, Robert

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DeepSVP: integration of genotype and phenotype for structural variant prioritization using deep learning od Althagafi, Azza, Alsubaie, Lamia, Kathiresan, Nagarajan, Mineta, Katsuhiko, Aloraini, Taghrid, Al Mutairi, Fuad, Alfadhel, Majid, Gojobori, Takashi, Alfares, Ahmad, Hoehndorf, Robert

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EMC10 homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay od Umair, Muhammad, Ballow, Mariam, Asiri, Abdulaziz, Alyafee, Yusra, al Tuwaijri, Abeer, Alhamoudi, Kheloud M., Aloraini, Taghrid, Abdelhakim, Marwa, Althagafi, Azza Thamer, Kafkas, Senay, Alsubaie, Lamia, Alrifai, Muhammad Talal, Hoehndorf, Robert, Alfares, Ahmed, Alfadhel, Majid

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What is the right sequencing approach? Solo VS extended family analysis in consanguineous populations od Alfares, Ahmed, Alsubaie, Lamia, Aloraini, Taghrid, Alaskar, Aljoharah, Althagafi, Azza, Alahmad, Ahmed, Rashid, Mamoon, Alswaid, Abdulrahman, Alothaim, Ali, Eyaid, Wafaa, Ababneh, Faroug, Albalwi, Mohammed, Alotaibi, Raniah, Almutairi, Mashael, Altharawi, Nouf, Alsamer, Alhanouf, Abdelhakim, Marwa, Kafkas, Senay, Mineta, Katsuhiko, Cheung, Nicole, Abdallah, Abdallah, Büchmann-Møller, Stine, Fukasawa, Yoshinori, Zhao, Xiang, Rajan, Issaac, Hoehndorf, Robert, Al Mutairi, Fuad, Gojobori, Takashi, Alfadhel, Majid

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