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4篇 您的检索式:作者名="Helger"
    题名 作者 年代 出处 被引量
1A Post‐Hoc Comparison of the Utility of S anger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases显示文摘Kornelia Neveling Ilse Feenstra Christian Gilissen Lies H. Hoefsloot Erik‐Jan Kamsteeg Arjen R. Mensenkamp Richard J. T. Rodenburg Helger G. Yntema Liesbeth Spruijt Sascha Vermeer Tuula Rinne Koen L. Gassen Danielle Bodmer Dorien Lugtenberg Rick Reuver We 2013Human Mutation2013,,12:1
2Cancer risk and genotype–phenotype correlations in PTEN hamartoma tumor syndrome显示文摘Marry H. Nieuwenhuis C. Marleen Kets Maureen Murphy-Ryan Helger G. Yntema D. Gareth Evans Chrystelle Colas Pal M?ller Frederik J. Hes Shirley V. Hodgson Maran J. W. Olderode-Berends Stefan Aretz Karl Heinimann Encarna B. Gómez García Fiona Douglas Allan S 2014Familial Cancer2014,,1:1
3On the equivalence of gravimetric PMdata with TEOM and beta-attenuation Measure-ments显示文摘Helger H Axel B Bostjan G 2004Journal of Aerosol Science2004,,35:1
4Prevalence of fragile X syndrome in males and females in Indonesia显示文摘AIM: To investigate the prevalence of fragile X syndrome(FXS) in intellectually disabled male and female Indonesians.METHODS: This research is an extension of a previously reported study on the identification of chromosomal aberrations in a large cohort of 527 Indonesians with intellectual disability(ID). In this previous study,87 patients had a chromosomal abnormality, five of whom expressed fragile sites on Xq27.3. Since FXS cannot always be identified by cytogenetic analysis, molecular testing of the fragile X mental retardation 1 CGG repeat was performed in 440 samples. The testing was also conducted in the five previously identified samples to confirm the abnormality. In total, a molecular study was conducted in 445 samples(162 females and 283 males).RESULTS: In the cohort of Indonesian ID population, the prevalence of FXS is 9/527(1.7%). The prevalence in males and females is 1.5%(5/329) and 2%(4/198), respectively. Segregation analysis in the families and X-inactivation studies were performed. We performed the first comprehensive genetic survey of a representative sample of male and female ID individuals from institutions and special schools in Indonesia. Our findings show that a comprehensive study of FXS can be performed in a developing country like Indonesia where diagnostic facilities are limited.CONCLUSION: The prevalence of FXS is equal in females and males in our study, which suggests that the prevalence of FXS in females could be underestimated.Farmaditya EP Mundhofir Tri I Winarni Willy Nillesen Bregje WM van Bon Marga Schepens Martina Ruiterkamp-Versteeg Ben CJ Hamel Helger G Yntema Sultana MH Faradz 2012World Journal of Medical Genetics2012,2,3:0
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