Zobrazeno 1 - 10
of 181
pro vyhledávání: '"Khodjet El Khil A"'
Autor:
Shaza Alkhidir, Karen El-Akouri, Nader Al-Dewik, Houssein Khodjet-El-khil, Sarah Okashah, Nazmul Islam, Tawfeg Ben-Omran, Mashael Al-Shafai
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-16 (2024)
Abstract Hearing loss is the most predominant sensory defect occurring in pediatrics, of which, 66% cases are attributed to genetic factors. The prevalence of hereditary hearing loss increases in consanguineous populations, and the prevalence of hear
Externí odkaz:
https://doaj.org/article/a5b78ae7fd3746b39dd5edc2d75c9ff8
Autor:
Abiib, Sumaya 1, Khodjet-El-khil, Houssein 1, El-Akouri, Karen 2, 3, Bux, Reem Ibrahim 2, Rezoug, Zoulikha 1, Abualainin, Wafa 4, Alkowari, Moza 4, Musa, Sara Osman 2, 3, Al Mulla, Mariam 2, 3, Al Saleh, Rehab 2, 3, Shahbeck, Noora 2, 3, Farag, Maria 3, Ismail, Said I. 5, Al Sulaiman, Reem 6, Ben-Omran, Tawfeg 2, 3, Al-Thani, Asma 1, 7, Al-Shafai, Mashael 1, 7, ∗
Publikováno v:
In Genetics in Medicine Open 2024 2 Supplement 2
Autor:
Sumaya Abiib, Houssein Khodjet-El-khil, Karen El-Akouri, Reem Ibrahim Bux, Zoulikha Rezoug, Wafa Abualainin, Moza Alkowari, Sara Osman Musa, Mariam Al Mulla, Rehab Al Saleh, Noora Shahbeck, Maria Farag, Said I. Ismail, Reem Al Sulaiman, Tawfeg Ben-Omran, Asma Al-Thani, Mashael Al-Shafai
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101866- (2024)
Genetic counseling is a dynamic and rapidly growing field. In Qatar, the significance of genetic counseling is underscored by the distinctive demographic characteristics of the population, including elevated rates of consanguinity and larger family s
Externí odkaz:
https://doaj.org/article/78de2d8c5ab34641b741d4491bdb42ad
Autor:
Sarra Elkamel, Sofia L. Marques, Luis Alvarez, Veronica Gomes, Sami Boussetta, Soufia Mourali-Chebil, Houssein Khodjet-El-Khil, Lotfi Cherni, Amel Benammar-Elgaaied, Maria J. Prata
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract To obtain refreshed insights into the paternal lineages of Tunisian populations, Y-chromosome diversity was assessed in two populations belonging to an Arab genealogical lineage, Kairouan and Wesletia, as well as in four Tunisian Andalusian
Externí odkaz:
https://doaj.org/article/749e912f28314418ba7aa6763a6b8601
Akademický článek
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Autor:
Hocine Badache, Sami Boussetta, Amel Benammar Elgaaeid, Lotfi Cherni, Houssein Khodjet El-khil
Publikováno v:
Annals of Human Biology, Vol 46, Iss 2, Pp 150-159 (2019)
Background: In Algeria, as in all North Africa, Berbers constitute the old background of the population. Today, Berber speakers account for only ∼ 25% of Algerians. This decline is the product of a complex human settlement from pre-history to recen
Externí odkaz:
https://doaj.org/article/1c0a1593336c4bedbc4442bdefad6a93
Autor:
Khodjet El Khil, Lilia
Publikováno v:
Revista de drept maritim / Journal of maritime law. (01-02):125-143
Externí odkaz:
https://www.ceeol.com/search/article-detail?id=1072878
Autor:
Sarra Elkamel, Lotfi Cherni, Luis Alvarez, Sofia L. Marques, Maria J. Prata, Sami Boussetta, Amel Benammar-Elgaaied, Houssein Khodjet-El-Khil
Publikováno v:
Annals of Human Biology, Vol 44, Iss 2, Pp 180-190 (2017)
Background: Recent genomic analyses suggest that the current North African gene pool was mainly influenced by population flow coming from the East that altered the genetic structure of autochthonous Berber populations. Such genetic flow has not been
Externí odkaz:
https://doaj.org/article/c398e71a26b3469d9ec3c94ad48edace
Publikováno v:
In Forensic Science International: Genetics July 2016 23:153-158
Akademický článek
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