Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Hana A. Al-Hakami"'
Autor:
Zuhair N. Al-Hassnan, Waad Albawardi, Faten Almutairi, Rawan AlMass, Albandary AlBakheet, Osama M. Mustafa, Laila AlQuait, Zarghuna M. A. Shinwari, Salma Wakil, Mustafa A. Salih, Majid Al-Fayyadh, Saeed M. Hassan, Mansour Aljoufan, Osima Al-Nakhli, Brynn Levy, Balsam AlMaarik, Hana A. Al-Hakami, Maysoon Alsagob, Dilek Colak, Namik Kaya
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-11 (2018)
Abstract Background Quick genetic diagnosis of a patient with congenital heart disease (CHD) is quite important for proper health care and management. Copy number variations (CNV), chromosomal imbalances and rearrangements have been frequently associ
Externí odkaz:
https://doaj.org/article/238fd9ac89634a798995c2454c74671b
Autor:
Balsam AlMaarik, Laila AlQuait, Mansour Aljoufan, Saeed Hassan, Albandary Al-Bakheet, Dilek Colak, Namik Kaya, Faten B. Almutairi, Maysoon Alsagob, Brynn Levy, Zuhair N. Al-Hassnan, Hana A. Al-Hakami, Rawan Almass, Majid Al-Fayyadh, Zarghuna M.A. Shinwari, Salma M. Wakil, Osama M. Mustafa, Waad Albawardi, Osima Al-Nakhli, Mustafa A. Salih
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-11 (2018)
Molecular Cytogenetics
Molecular Cytogenetics
Background Quick genetic diagnosis of a patient with congenital heart disease (CHD) is quite important for proper health care and management. Copy number variations (CNV), chromosomal imbalances and rearrangements have been frequently associated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e78ccaa91806d95206c08a0660f06a62
https://doi.org/10.1186/s13039-018-0356-6
https://doi.org/10.1186/s13039-018-0356-6