Zobrazeno 1 - 10
of 57
pro vyhledávání: '"K. K. Naguib"'
Publikováno v:
Eastern Mediterranean Health Journal. 15:345-352
We studied 21 patients with Sanjad-Sakati syndrome (SSS) from 16 families. Parental consanguinity was recorded in 2 families (12.5%). All patients had severe intrauterine growth retardation, short stature, small hands and feet, blue sclera, deep-set
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e987895c41ef30bd15a23916f49a67e
https://doi.org/10.26719/2009.15.2.345
https://doi.org/10.26719/2009.15.2.345
Autor:
T. I. Farag, A. S. Teebi, M. Y. El-Khalifa, Mohamed A.A. Moussa, S. A. Al-Awadi, K. K. Naguib
Publikováno v:
Clinical Genetics. 29:384-388
A stratified representative sample size of 5,007 Kuwaiti females aged 15 years and above was drawn during 1983 and structurally interviewed to study the influence of consanguineous marriages (up to the second cousin) on reproductive wastage. Losses c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0799e5bba06f6ab4fd35342a7a13fae3
https://doi.org/10.1111/j.1399-0004.1986.tb00509.x
https://doi.org/10.1111/j.1399-0004.1986.tb00509.x
Autor:
M. Y. El-Khalifa, K. K. Naguib, Ahmad S. Teebi, Talaat I. Farag, el-Dossary L, Mohamed A.A. Moussa, S. A. Al-Awadi
Publikováno v:
Clinical Genetics. 27:483-486
A total of 5,007 Kuwaitis were ascertained to study the incidence of consanguineous marriages during 1983. The rate of consanguineous mating was found to be 54.3% with estimated population incidence rates 52.9 to 55.7%. First cousin marriages were th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27115fbe84270e5330fa955f241ec9c7
https://doi.org/10.1111/j.1399-0004.1985.tb00236.x
https://doi.org/10.1111/j.1399-0004.1985.tb00236.x
Publikováno v:
Eastern Mediterranean Health Journal. 10:116-124
In a prospective study in Kuwait, 182 mentally retarded male patients who fulfilled 5 or more clinical criteria of fragile X syndrome were screened using polymerase chain reaction [PCR] testing. Twenty patients [11%] were highly suspected of having f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94fb8025753e927bc57ffc548e20bd5c
https://doi.org/10.26719/2004.10.1-2.116
https://doi.org/10.26719/2004.10.1-2.116
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:
Hanaa Ismail, Hassan Sallam, Shawky Mahmoud Tayel, Abdel Rahman Abd Rabuh, K. K. Naguib, Sally Tayel
Publikováno v:
The FASEB Journal. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e946c42bb78fe9e4789f65751c7d2c62
https://doi.org/10.1096/fasebj.26.1_supplement.908.6
https://doi.org/10.1096/fasebj.26.1_supplement.908.6
Publikováno v:
Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit. 15(2)
We studied 21 patients with Sanjad-Sakati syndrome (SSS) from 16 families. Parental consanguinity was recorded in 2 families (12.5%). All patients had severe intrauterine growth retardation, short stature, small hands and feet, blue sclera, deep-set
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::af41f6133e0fe00d7e60656e80779dac
https://pubmed.ncbi.nlm.nih.gov/19554981
https://pubmed.ncbi.nlm.nih.gov/19554981
Publikováno v:
Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit. 13(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5ed3d259f0fd30069fb3fa9c8d41d540
https://pubmed.ncbi.nlm.nih.gov/17955782
https://pubmed.ncbi.nlm.nih.gov/17955782
Autor:
S. M. Tayel, Fawziah M A Mohammed, Fatma I. Al-Yatama, K. K. Naguib, S. Gouda, Maie D. Al-Bader
Publikováno v:
Andrologia. 39(3)
Infertility is one of the major public health problems, affecting 15% of couples who attempt pregnancy; in 50% of these, the male partner is responsible. Chromosomal abnormalities and Y microdeletions in the azoospermia factor (AZF) region are known
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d58c0677d683595ebfdde44aeb3e069
https://pubmed.ncbi.nlm.nih.gov/17683468
https://pubmed.ncbi.nlm.nih.gov/17683468
Publikováno v:
Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit. 10(4-5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ab56ae5e5d5ac700519967e531e03285
https://pubmed.ncbi.nlm.nih.gov/16335663
https://pubmed.ncbi.nlm.nih.gov/16335663