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Khalid Hama Salih

Showing results (1-10 of 6) with videos related to

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Sage Open Pediatrics|July 4, 2025
Vancomycin Resistance <i>Streptococcus pneumoniae</i>, a Case ReportZana Baqi Najmadden, Khalid Hama Salih, Jihad Ibrahim Hama, et al.
Frontiers in Immunology|February 12, 2019
A Syrian Refugee in Iraq Diagnosed as a Case of IL12RB1 Deficiency in Japan Using Dried Blood SpotsLika'a Fasih Y Al-Kzayer, Ahmed K Yassin, Khalid Hama Salih, et al.
Global Pediatric Health|November 8, 2024
Outbreak of Meningitis in Iraq in 2023Khalid Hama Salih, Zana Baqi Najmadden, Bahadin Qader Ahmed, et al.
Genes|January 21, 2023
Genetic Insights from Consanguineous Cardiomyopathy FamiliesConstance Maurer, Olga Boleti, Paria Najarzadeh Torbati, et al.
American Journal of Human Genetics|February 24, 2026
Bi-allelic variants in NRDC cause a neurodevelopmental disorder characterized by neonatal lethality, microcephaly, and brain abnormalitiesDavut Pehlivan, Abigail Sandoval, Reza Maroofian, et al.
European Journal of Human Genetics : EJHG|October 18, 2024
Epigenomic and phenotypic characterization of DEGCAGS syndromeKarim Karimi, Denisa Weis, Ingvild Aukrust, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Sage Open Pediatrics|July 4, 2025
Vancomycin Resistance <i>Streptococcus pneumoniae</i>, a Case ReportZana Baqi Najmadden, Khalid Hama Salih, Jihad Ibrahim Hama, et al.
Frontiers in Immunology|February 12, 2019
A Syrian Refugee in Iraq Diagnosed as a Case of IL12RB1 Deficiency in Japan Using Dried Blood SpotsLika'a Fasih Y Al-Kzayer, Ahmed K Yassin, Khalid Hama Salih, et al.
Global Pediatric Health|November 8, 2024
Outbreak of Meningitis in Iraq in 2023Khalid Hama Salih, Zana Baqi Najmadden, Bahadin Qader Ahmed, et al.
Genes|January 21, 2023
Genetic Insights from Consanguineous Cardiomyopathy FamiliesConstance Maurer, Olga Boleti, Paria Najarzadeh Torbati, et al.
American Journal of Human Genetics|February 24, 2026
Bi-allelic variants in NRDC cause a neurodevelopmental disorder characterized by neonatal lethality, microcephaly, and brain abnormalitiesDavut Pehlivan, Abigail Sandoval, Reza Maroofian, et al.
European Journal of Human Genetics : EJHG|October 18, 2024
Epigenomic and phenotypic characterization of DEGCAGS syndromeKarim Karimi, Denisa Weis, Ingvild Aukrust, et al.
Pageof 1