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1 . Academic Journal
NOD2/CARD15 polymorphisms (P268S, IVS8+158, G908R, L1007fs, R702W) among Kuwaiti patients with Crohn's disease: A case-control study
저자
by
Hassan Abdelnaby
;
Ndeye Coumba Ndiaye
;
Ferdinando D'Amico
;
Ahmed Mahmoud Fouad
;
Sameh Hassan
, et al.
소스
The Saudi Journal of Gastroenterology, Vol 27, Iss 4, Pp 249-256 (2021)
Open Access (DOAJ)
Web of Science
Scopus
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7 . Academic Journal
Mutation spectrum analysis of Duchenne/Becker muscular dystrophy in 68 families in Kuwait: The era of personalized medicine.
저자
by
Fawziah Mohammed
;
Alaa Elshafey
;
Haya Al-Balool
;
Hayat Alaboud
;
Mohammed Al Ben Ali
, et al.
소스
PLoS ONE, Vol 13, Iss 5, p e0197205 (2018)
Open Access (DOAJ)
Web of Science
Scopus
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7 .
NOD2/CARD15 polymorphisms (P268S, IVS8+158, G908R, L1007fs, R702W) among Kuwaiti patients with Crohn's disease: A case-control study
저자
by
Mohammed Faisal
;
Wafaa Al Hashash
;
Yousef Alshamali
;
Laurent Peyrin-Biroulet
;
Ferdinando D'Amico
, et al.
소스
The Saudi Journal of Gastroenterology, Vol 27, Iss 4, Pp 249-256 (2021)
Saudi Journal of Gastroenterology : Official Journal of the Saudi Gastroenterology Association
Open Access (OpenAIRE)
Web of Science
Scopus
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7 .
Woodhouse–Sakati syndrome in six Kuwaiti families
저자
by
Hayat Al-Aboud
;
Laila Bastaki
;
Sayed Gouda
;
Amal Al-Wadaani
;
Alaa Elshafey
.
소스
Middle East Journal of Medical Genetics
. 2:39-44
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7 .
Mutation spectrum analysis of Duchenne/Becker muscular dystrophy in 68 families in Kuwait: The era of personalized medicine
저자
by
Mohammed Ali
;
Laila Bastaki
;
Adel Baqer
;
Fawziah M A Mohammed
;
Alaa Elshafey
, et al.
소스
PLoS ONE
PLoS ONE, Vol 13, Iss 5, p e0197205 (2018)
Open Access (OpenAIRE)
Web of Science
Scopus
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7 .
Molecular and Clinical Evaluation of Primary Congenital Glaucoma in Kuwait
저자
by
Sadiqa Al-Awadi
;
Abdulmutalib H. Behbehani
;
Alaa Elshafey
;
Sidky M.A. Abdelmoaty
;
Suad AlFadhli
.
소스
American Journal of Ophthalmology
. 141:512-516
Web of Science
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7 .
Erratum: The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions
저자
by
Ramesh Reddy
;
Ngoc M P Nguyen
;
Guillaume Sarrabay
;
Maryam Rezaei
;
Mayra C G Rivas
, et al.
소스
European Journal of Human Genetics
. 24:1516-1516
Open Access (OpenAIRE)
Web of Science
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7 .
Impact of 226CT MSH2 gene mutation on cancer phenotypes in two HNPCC-associated highly-consanguineous families from Kuwait: emphasis on premarital genetic testing
저자
by
Fatemah Al-Mosawi
;
Waleed Al-Ali
;
Sadiqa Al-Awadi
;
Alaa Elshafey
;
Fahd Al-Mulla
, et al.
소스
Familial cancer
. 8(4)
Full Text (Springer)
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7 .
Molecular characterization of glucose-6-phosphate dehydrogenase gene defect in the Kuwaiti population
저자
by
Matra Salim
;
Anwar AlAwadi
;
Layla Bastaki
;
Alaa Elshafey
;
Salim Kaaba
, et al.
소스
Archives of pathologylaboratory medicine
. 129(9)
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7 .
Hypothyroidism-retardation-dysmorphism (HRD): Is there a new variant not caused by a TBCE mutation?
저자
by
Fawziah Mohammad
;
Sayed Gouda
;
Alaa Elshafey
;
Kamal Naguib
.
소스
American Journal of Medical Genetics Part A
. :301-302
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