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Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-81 Sentence denotes Skewed X inactivation in a female MZ twin results in Duchenne muscular dystrophy.
T1 0-81 Sentence denotes Skewed X inactivation in a female MZ twin results in Duchenne muscular dystrophy.
TextSentencer_T2 82-139 Sentence denotes One of female MZ twins presented with muscular dystrophy.
T2 82-139 Sentence denotes One of female MZ twins presented with muscular dystrophy.
TextSentencer_T3 140-266 Sentence denotes Physical examination, creatine phosphokinase levels, and muscle biopsy were consistent with Duchenne muscular dystrophy (DMD).
T3 140-266 Sentence denotes Physical examination, creatine phosphokinase levels, and muscle biopsy were consistent with Duchenne muscular dystrophy (DMD).
TextSentencer_T4 267-354 Sentence denotes However, because of her sex she was diagnosed as having limb-girdle muscular dystrophy.
T4 267-354 Sentence denotes However, because of her sex she was diagnosed as having limb-girdle muscular dystrophy.
TextSentencer_T5 355-448 Sentence denotes With cDNA probes to the DMD gene, a gene deletion was detected in the twins and their mother.
T5 355-448 Sentence denotes With cDNA probes to the DMD gene, a gene deletion was detected in the twins and their mother.
TextSentencer_T6 449-593 Sentence denotes The de novo mutation which arose in the mother was shown by novel junction fragments generated by HindIII, PstI, or TaqI when probed with cDNA8.
T6 449-593 Sentence denotes The de novo mutation which arose in the mother was shown by novel junction fragments generated by HindIII, PstI, or TaqI when probed with cDNA8.
TextSentencer_T7 594-765 Sentence denotes Additional evidence of a large gene deletion was given by novel SfiI junction fragments detected by probes p20, J-Bir, and J-66 on pulsed-field gel electrophoresis (PFGE).
T7 594-765 Sentence denotes Additional evidence of a large gene deletion was given by novel SfiI junction fragments detected by probes p20, J-Bir, and J-66 on pulsed-field gel electrophoresis (PFGE).
TextSentencer_T8 766-874 Sentence denotes Immunoblot analysis of muscle from the affected twin showed dystrophin of normal size but of reduced amount.
T8 766-874 Sentence denotes Immunoblot analysis of muscle from the affected twin showed dystrophin of normal size but of reduced amount.
TextSentencer_T9 875-1012 Sentence denotes Immunofluorescent visualization of dystrophin revealed foci of dystrophin-positive fibers adjacent to foci of dystrophin-negative fibers.
T9 875-1012 Sentence denotes Immunofluorescent visualization of dystrophin revealed foci of dystrophin-positive fibers adjacent to foci of dystrophin-negative fibers.
TextSentencer_T10 1013-1174 Sentence denotes These data indicate that the affected twin is a manifesting carrier of an abnormal DMD gene, her myopathy being a direct result of underexpression of dystrophin.
T10 1013-1174 Sentence denotes These data indicate that the affected twin is a manifesting carrier of an abnormal DMD gene, her myopathy being a direct result of underexpression of dystrophin.
TextSentencer_T11 1175-1299 Sentence denotes Cytogenetic analysis revealed normal karyotypes, eliminating the possibility of a translocation affecting DMD gene function.
T11 1175-1299 Sentence denotes Cytogenetic analysis revealed normal karyotypes, eliminating the possibility of a translocation affecting DMD gene function.
TextSentencer_T12 1300-1492 Sentence denotes Both linkage analysis and DNA fingerprint analysis revealed that each twin has two different X chromosomes, eliminating the possibility of uniparental disomy as a mechanism for DMD expression.
T12 1300-1492 Sentence denotes Both linkage analysis and DNA fingerprint analysis revealed that each twin has two different X chromosomes, eliminating the possibility of uniparental disomy as a mechanism for DMD expression.
TextSentencer_T13 1493-1727 Sentence denotes On the basis of methylation differences of the paternal and maternal X chromosomes in these MZ twins, we propose uneven lyonization (X chromosome inactivation) as the underlying mechanism for disease expression in the affected female.
T13 1493-1727 Sentence denotes On the basis of methylation differences of the paternal and maternal X chromosomes in these MZ twins, we propose uneven lyonization (X chromosome inactivation) as the underlying mechanism for disease expression in the affected female.