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PubMed:1357962 JSONTXT 14 Projects

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Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-99 Sentence denotes Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.
T1 0-99 Sentence denotes Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.
TextSentencer_T2 100-212 Sentence denotes Uniparental disomy has recently been recognized to cause human disorders, including Prader-Willi syndrome (PWS).
T2 100-212 Sentence denotes Uniparental disomy has recently been recognized to cause human disorders, including Prader-Willi syndrome (PWS).
TextSentencer_T3 213-436 Sentence denotes We describe a particularly instructive case which raises important issues concerning the mechanisms producing uniparental disomy and whose evaluation provides evidence that trisomy may precede uniparental disomy in a fetus.
T3 213-436 Sentence denotes We describe a particularly instructive case which raises important issues concerning the mechanisms producing uniparental disomy and whose evaluation provides evidence that trisomy may precede uniparental disomy in a fetus.
TextSentencer_T4 437-586 Sentence denotes Chorionic villus sampling performed for advanced maternal age revealed trisomy 15 in all direct and cultured cells, though the fetus appeared normal.
T4 437-586 Sentence denotes Chorionic villus sampling performed for advanced maternal age revealed trisomy 15 in all direct and cultured cells, though the fetus appeared normal.
TextSentencer_T5 587-676 Sentence denotes Chromosome analysis of amniocytes obtained at 15 wk was normal in over 100 cells studied.
T5 587-676 Sentence denotes Chromosome analysis of amniocytes obtained at 15 wk was normal in over 100 cells studied.
TextSentencer_T6 677-840 Sentence denotes The child was hypotonic at birth, and high-resolution banding failed to reveal the deletion of 15q11-13, a deletion which is found in 50%-70% of patients with PWS.
T6 677-840 Sentence denotes The child was hypotonic at birth, and high-resolution banding failed to reveal the deletion of 15q11-13, a deletion which is found in 50%-70% of patients with PWS.
TextSentencer_T7 841-886 Sentence denotes Over time, typical features of PWS developed.
T7 841-886 Sentence denotes Over time, typical features of PWS developed.
TextSentencer_T8 887-970 Sentence denotes Molecular genetic analysis using probes for chromosome 15 revealed maternal disomy.
T8 887-970 Sentence denotes Molecular genetic analysis using probes for chromosome 15 revealed maternal disomy.
TextSentencer_T9 971-1236 Sentence denotes Maternal nondisjunction with fertilization of a disomic egg by a normal sperm, followed by loss of the paternal 15, is a likely cause of confined placental mosaicism and uniparental disomy in this case of PWS, and advanced maternal age may be a predisposing factor.
T9 971-1236 Sentence denotes Maternal nondisjunction with fertilization of a disomic egg by a normal sperm, followed by loss of the paternal 15, is a likely cause of confined placental mosaicism and uniparental disomy in this case of PWS, and advanced maternal age may be a predisposing factor.