Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nayerossadat Nouri"'
Autor:
Maryam Sedghi, Elham Esfandiari, Esmat Fazel-Najafabadi, Mansoor Salehi, Abbas Salavaty, Shirin Fattahpour, Leila Dehghani, Nayerossadat Nouri, Fariborz Mokarian
Publikováno v:
Journal of Research in Medical Sciences, Vol 21, Iss 1, Pp 95-95 (2016)
Background: The second leading cause of cancer deaths in women is breast cancer. Germline mutations in susceptibility breast cancer gene BRCA1 increase the lifetime risk of breast cancer. Eighty-one large genomic rearrangements (LGRs) have been repor
Externí odkaz:
https://doaj.org/article/8654155a4a494c7295facd4f06c78169
Publikováno v:
Advanced Biomedical Research, Vol 1, Iss 1, Pp 14-14 (2012)
Developmental stuttering is a common disorder of speech dissiliency that is characterized by excessive repetitions of sounds, syllables, and monosyllabic words, as well as sound prolongations and complete blockages of the vocal tract. About 60 millio
Externí odkaz:
https://doaj.org/article/c3a11229618749f5af1826a2f9630226
Autor:
F Jafary, T Gholamrezapour, Mansour Salehi, Nayerossadat Nouri, Majid Hosseinzadeh, Maryam Sedghi, Zakiye Nadeali
Publikováno v:
Молекулярная биология. 49:949-952
According to previous studies the IRF6rs2235371 polymorphism is a risk factor for NSCL/P in different populations. However our recent study revealed no correlation between IRF6rs642961 and NSCL/P in our population. In the present study we have invest
Autor:
Elham Esfandiari, Fariborz Mokarian, Nayerossadat Nouri, Mansoor Salehi, Abbas Salavaty, Maryam Sedghi, Esmat Fazel-Najafabadi, Shirin Fattahpour, Leila Dehghani
Publikováno v:
Journal of Research in Medical Sciences, Vol 21, Iss 1, Pp 95-95 (2016)
Scopus-Elsevier
Journal of Research in Medical Sciences : The Official Journal of Isfahan University of Medical Sciences
Scopus-Elsevier
Journal of Research in Medical Sciences : The Official Journal of Isfahan University of Medical Sciences
Background: Th e second leading cause of cancer deaths in women is breast cancer. Germline mutations in susceptibility breast cancer gene BRCA1 increase the lifetime risk of breast cancer. Eighty-one large genomic rearrangements (LGRs) have been repo
Publikováno v:
Advanced Biomedical Research
Advanced Biomedical Research, Vol 1, Iss 1, Pp 14-14 (2012)
Advanced Biomedical Research, Vol 1, Iss 1, Pp 14-14 (2012)
Developmental stuttering is a common disorder of speech dissiliency that is characterized by excessive repetitions of sounds, syllables, and monosyllabic words, as well as sound prolongations and complete blockages of the vocal tract. About 60 millio
Autor:
Nayerossadat Nouri, Nargesossadat Nouri, Aryani, Omid, Kamalidehghan, Behnam, Houshmand, Massoud
Publikováno v:
Scopus-Elsevier
Background: Mucopolysaccharidosis type-VI (MPS-VI), which is inherited as an autosomal recessive trait, results from the deficiency of N-acetylgalactosamine 4-sulfatase (arylsulfatase B) activity and the lysosomal accumulation of dermatan sulfate. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e73aac8f82df2d542bcac859835cad61
http://www.scopus.com/inward/record.url?eid=2-s2.0-84879429623&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84879429623&partnerID=MN8TOARS
Autor:
Nayerossadat N; Molecular Genetic Laboratory, Alzahra Hospital, Isfahan University of Medical Sciences, Isfahan, Iran ; Pediatric Inherited Disease Research Center, Isfahan University of Medical Sciences, Isfahan, Iran., Maedeh T, Ali PA
Publikováno v:
Advanced biomedical research [Adv Biomed Res] 2012; Vol. 1, pp. 27. Date of Electronic Publication: 2012 Jul 06.