منابع مشابه
Prenatal sex determination in suspicious cases of X-linked recessive diseases by the amelogenin gene
Objective(s):To determine the fetal discernment in suspected cases of sex linked recessive disease in the first trimester of pregnancy. Materials and Methods: After collection of 100 Chorionic Villi samples, the DNAs were extracted and baby gender was determined. Meanwhile, after increasing the sensitivity, the system was able to detect the sex of each cell which was obtained by biopsy. Resul...
متن کاملElectrophoretic Variation for X-chromosome-linked Phosphoglycerate
Electrophoretic variation €or X-chromosome-linked phosphoglycerate kinase (PGK-1) has been found as a polymorphism in feral mice in Denmark. Males from feral sampling or from a variety of genetic crosses have only a single-banded phenotype of the variant PGK-1A type or of the PGK-IB type commonly found among inbred mice. By contrast, three phenotypes were observed among females; two honozygous ...
متن کاملprenatal sex determination in suspicious cases of x-linked recessive diseases by the amelogenin gene
objective(s):to determine the fetal discernment in suspected cases of sex linked recessive disease in the first trimester of pregnancy. materials and methods: after collection of 100 chorionic villi samples, the dnas were extracted and baby gender was determined. meanwhile, after increasing the sensitivity, the system was able to detect the sex of each cell which was obtained by biopsy. results...
متن کاملA novel missense mutation (p.P52R) in amelogenin gene causing X-linked amelogenesis imperfecta.
Amelogenesis imperfecta (AI) is a hereditary disease with abnormal dental enamel formation. Here we report a Japanese family with X-linked AI transmitted over at least four generations. Mutation analysis revealed a novel mutation (p.P52R) in exon 5 of the amelogenin gene. The mutation was detected as heterozygous in affected females and as hemizygous in their affected father. The affected siste...
متن کاملPrenatal sex determination in suspicious cases of X-linked recessive diseases by the amelogenin gene
OBJECTIVE(S) To determine the fetal discernment in suspected cases of sex linked recessive disease in the first trimester of pregnancy. MATERIALS AND METHODS After collection of 100 Chorionic Villi samples, the DNAs were extracted and baby gender was determined. Meanwhile, after increasing the sensitivity, the system was able to detect the sex of each cell which was obtained by biopsy. RESU...
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ژورنال
عنوان ژورنال: International Journal of Research in Medical Sciences
سال: 2017
ISSN: 2320-6012,2320-6071
DOI: 10.18203/2320-6012.ijrms20174549