Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Amir Dabboul"'
Autor:
Hossam Murad, Mohamad Baseel Alhalabi, Amir Dabboul, Nour Alfakseh, Mohamad Sayah Nweder, Youssef Zghib, Hala Wannous
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-11 (2021)
Abstract Background Characterization of the molecular basis of primary hyperoxaluria type 1 (PH-1) in Syria has been accomplished through the analysis of 90 unrelated chromosomes from 45 Syrians patients with PH-1 from different regions. Methods Alan
Externí odkaz:
https://doaj.org/article/ba8ed58a920f426d862534e29768b23b
Autor:
Youssef Zghib, Nour Alfakseh, Hossam Murad, Amir Dabboul, Mohamad Sayah Nweder, Mohamad Baseel Alhalabi, Hala Wannous
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-11 (2021)
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-11 (2021)
Background Characterization of the molecular basis of primary hyperoxaluria type 1 (PH-1) in Syria has been accomplished through the analysis of 90 unrelated chromosomes from 45 Syrians patients with PH-1 from different regions. Methods Alanine glyox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34faa45045ff6cddf1067965885c1f85
https://pubmed.ncbi.nlm.nih.gov/34082749
https://pubmed.ncbi.nlm.nih.gov/34082749
Autor:
Rami A. Jarjour, Faten Moasses, Amir Dabboul, Yasser Mukhalalaty, Walid Al-Achkar, Hossam Murad, Ahmad Omar Bakoor
Publikováno v:
Hematology. 23:697-704
Objectives β-Thalassemia disease is caused by mutations in the β-globin gene. This is considered as one of the common genetic disorders in Syria. The aim of this study was to identify the geographical distribution of the β-thalassemia mutations in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8036b3fd6c060f34e8390e0ffc12f3d
https://doi.org/10.1080/10245332.2018.1461291
https://doi.org/10.1080/10245332.2018.1461291
Publikováno v:
Gene. 528(2)
Characterization of the molecular basis of phenylketonuria (PKU) in Syria has been accomplished through the analysis of 78 unrelated chromosomes from 39 Syrian patients with PKU. Phenylalanine hydroxylase (PAH) gene mutations have been analyzed by us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d86f8fb4be1521048e19e7e35a4c72b
https://pubmed.ncbi.nlm.nih.gov/23856132
https://pubmed.ncbi.nlm.nih.gov/23856132