Zobrazeno 1 - 7
of 7
pro vyhledávání: '"M A, Redha"'
Autor:
M. Alfar Redha
Publikováno v:
Al-Adl, Vol 15, Iss 1, Pp 106-131 (2023)
Marriage certificates are usually given to husbands and wives who have entered into a marriage contract according to Islam but are not legally registered by the state. In the end, the marriage has no legal force. As a result, when a problem arises in
Externí odkaz:
https://doaj.org/article/744a04b5ec73493f8cb7f0f2e8e417c6
Autor:
AbdelKhalek Abdelnabi, Amr, Fawaz S. Al-Qahtani, Fawaz, Redha M. Radaydeh, Redha, Mohammed Shaqfeh, Mohamed, Raed F. Manna, Raed
Publikováno v:
IMDEA Networks Institute Digital Repository
IMDEA Networks Institute
instname
IMDEA Networks Institute
instname
This paper presents new approaches to characterize the achieved performance of hybrid control-access small cells in the context of two-tier multi-input multi-output (MIMO) cellular networks with random interference distributions. The hybrids cheme at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::afc262198743668bac95a87f4e26a9fc
http://hdl.handle.net/20.500.12761/464
http://hdl.handle.net/20.500.12761/464
Autor:
R. A. Wahba, S. Al‐Hijji, Talaat I. Farag, E. A. Qurban, Lulwa A Aljeryan, Makia J. Marafie, B. Kasrawi, G. Yadav, I S al-Sulaiman, S. A. Al-Awadi, N. Al‐Hashash, M. Y. El-Khalifa, H. Al‐Aboud, F. M. Mohammed, D. S. Krishna Murthy, M. A. Redha, S. Abul Hassan, Laila Bastaki, M. H. El‐Badramary, A. A. Redha, M. A. Aref, H. Al‐Khorafi, D. Al‐Dighashem
Publikováno v:
Clinical Genetics. 44:329-334
Farag TI, Al-Awadi SA, El-Badramary MH, Aref MA, Kasrawi B, Krishna Murthy DS, El-Khalifa MY, Yadav G, Marafie MJ, Bastaki L, Wahba RA, Mohammed FM, Abul Hasan S, Redha AA, Redha MA, Al-aboud H, Al-Hijji S, Al-Dighashem D, Al-Hashash N, Al-Jeeryan L,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d528176dfb6bc2ec83d424ed6bc4b788
https://doi.org/10.1111/j.1399-0004.1993.tb03910.x
https://doi.org/10.1111/j.1399-0004.1993.tb03910.x
Autor:
S A Gouda, S M Tayel, Laila Bastaki, F Mustafa, S A Abulhassan, M. A. Redha, K. K. Naguib, S A Al-Awadi, Mohamed A.A. Moussa, D.S.K. Murthy
Publikováno v:
International Journal of Epidemiology. 28:711-716
Trisomy 18 (Edwards' syndrome, T18) is the second most common trisomy in man. We describe 118 children with regular T18 who were ascertained clinically and cytogenetically in the Kuwait Medical Genetics Centre during 1980-1997.Ascertainment of T18 ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ac221dafb5d6886cbaf3422153ef64e
https://doi.org/10.1093/ije/28.4.711
https://doi.org/10.1093/ije/28.4.711
Autor:
M A, Redha, D S, Krishna Murthy, S A, al-Awadi, I S, al-Sulaiman, M A, Sabry, S A, el-Bahey, T I, Farag
Publikováno v:
Annales de genetique. 39(1)
A 3-year-6-month old Lebanese female child with multiple congenital anomalies including, facial dysmorphism, prominent low set ears, micrognathia, anti-mongoloid palpebral fissures and psychomotor retardation was investigated. Her karyotype showed de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::12fb997f1f98cca00f4117e15346aecd
https://pubmed.ncbi.nlm.nih.gov/9297445
https://pubmed.ncbi.nlm.nih.gov/9297445
Publikováno v:
American journal of medical genetics. 36(1)
We report on apparently nonmosaic trisomy 22 in a liveborn girl with multiple congenital anomalies. The abnormalities were growth retardation; microcephaly; hypertelorism; epicanthic folds; anti-mongoloid slant; apparently low-set, malformed ears; hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abe2c7cba28fa3ba22121be38e8b53a1
https://pubmed.ncbi.nlm.nih.gov/2185636
https://pubmed.ncbi.nlm.nih.gov/2185636
Autor:
T I, Farag, D S, Krishna Murthy, S A, Al-Awadi, T S, Sundareshan, S A, Ai-Othman, S A, Mady, M A, Redha
Publikováno v:
Annales de genetique. 30(3)
Robertsonian translocations occur in about 2.5% of Down syndrome. We report here a Down syndrome with karyotype, 46,XX,-14,-22,+der t dic(14p;22p)pat, +21. Proband's father, two sisters, and a brother are phenotypically normal, heterozygous carriers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fabe4e6a58dec5d730e0d6c50b4f0e36
https://pubmed.ncbi.nlm.nih.gov/2960263
https://pubmed.ncbi.nlm.nih.gov/2960263