An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case
Wafa, Abdulsamad, Jarjour, Rami A, Aljapawe, Abdulmunim, ALmedania, Suher, Liehr, Thomas, Melo, Joana B, Carreira, Isabel M, Othman, Moneeb A K, Al-Achkar, Walid
Published in Molecular cytogenetics (10.07.2020)
Published in Molecular cytogenetics (10.07.2020)
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Journal Article
A new childhood ALL case with an extremely complex karyotype and acute spontaneous tumor lysis syndrome
Wafa, Abdulsamad, Jarjour, Rami A, Alolabi, Doaa, Liehr, Thomas, Hamdan, Othman, Melo, Joana B, Carreira, Isabel M, Othman, Moneeb A K, Al-Achkar, Walid
Published in Molecular cytogenetics (11.09.2020)
Published in Molecular cytogenetics (11.09.2020)
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Journal Article
Association of Methylenetetrahydrofolate Reductase C677T and A1298C Gene Polymorphisms With Recurrent Pregnancy Loss in Syrian Women
Al-Achkar, Walid, Wafa, Abdulsamad, Ammar, Samer, Moassass, Faten, Jarjour, Rami A.
Published in Reproductive sciences (Thousand Oaks, Calif.) (01.09.2017)
Published in Reproductive sciences (Thousand Oaks, Calif.) (01.09.2017)
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Geographical distribution of β-globin gene mutations in Syria
Murad, Hossam, Moasses, Faten, Dabboul, Amir, Mukhalalaty, Yasser, Bakoor, Ahmad Omar, Al-Achkar, Walid, Jarjour, Rami A.
Published in Hematology (Luxembourg) (21.10.2018)
Published in Hematology (Luxembourg) (21.10.2018)
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Spectrum of cystic fibrosis mutations in Syrian patients
Jarjour, Rami A, Al-Berrawi, Sumaya, Ammar, Samer, Majdalawi, Rami
Published in Minerva pediatrica (01.04.2018)
Published in Minerva pediatrica (01.04.2018)
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Journal Article
Molecular Update of β-Thalassemia Mutations in the Syrian Population: Identification of Rare β-Thalassemia Mutations
Jarjour, Rami A., Murad, Hossam, Moasses, Faten, Al-Achkar, Walid
Published in Hemoglobin (01.01.2014)
Published in Hemoglobin (01.01.2014)
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A novel heterozygous variant in exon 32 of the CHD7 gene (c.6923C>T) in a Syrian family with Kallmann syndrome
Wafa, Abdulsamad, Moassass, Faten, Almedani, Suher, Liehr, Thomas, Wilhelm, Kathleen, As'sad, Manar, Knippenberg, Sarah, Glaubitz, Ralf, Jarjour, Rami A., Achkar, Walid Al
Published in Research Results in Biomedicine (30.06.2020)
Published in Research Results in Biomedicine (30.06.2020)
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Journal Article
A new childhood ALL case with an extremely complex karyotype and acute spontaneous tumor lysis syndrome
Wafa, Abdulsamad, Jarjour, Rami A, Alolabi, Doaa, Liehr, Thomas, Hamdan, Othman, Melo, Joana B, Carreira, Isabel M, Othman, Moneeb A K, Al-Achkar, Walid
Published in Molecular cytogenetics (01.01.2020)
Published in Molecular cytogenetics (01.01.2020)
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An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case
Wafa, Abdulsamad, Jarjour, Rami A, Aljapawe, Abdulmunim, ALmedania, Suher, Liehr, Thomas, Melo, Joana B, Carreira, Isabel M, Othman, Moneeb A K, Al-Achkar, Walid
Published in Molecular cytogenetics (01.01.2020)
Published in Molecular cytogenetics (01.01.2020)
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