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PubMed:263442 JSONTXT 9 Projects

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Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-101 Sentence denotes Genetic aspects of the BOR syndrome--branchial fistulas, ear pits, hearing loss, and renal anomalies.
T1 0-101 Sentence denotes Genetic aspects of the BOR syndrome--branchial fistulas, ear pits, hearing loss, and renal anomalies.
TextSentencer_T2 102-326 Sentence denotes A pedigree of branchio-oto-renal dysplasia (the BOR syndrome) is reported, including the documentation by serial audiometric studies of the onset and rapid progression of hearing loss in the twin sister of an affected child.
T2 102-326 Sentence denotes A pedigree of branchio-oto-renal dysplasia (the BOR syndrome) is reported, including the documentation by serial audiometric studies of the onset and rapid progression of hearing loss in the twin sister of an affected child.
TextSentencer_T3 327-441 Sentence denotes The literature on this syndrome is analyzed to derive some figures for use in genetic counseling of such families.
T3 327-441 Sentence denotes The literature on this syndrome is analyzed to derive some figures for use in genetic counseling of such families.
TextSentencer_T4 442-765 Sentence denotes Branchio-oto-renal dysplasia is an autosomal dominant disorder in which affected individuals may have preauricular pits, lachrymal duct stenosis, hearing loss, branchial fistulas or cysts, structural defects of the outer, middle, and inner ear, and renal anomalies, which may range from mild hypoplasia to complete absence.
T4 442-765 Sentence denotes Branchio-oto-renal dysplasia is an autosomal dominant disorder in which affected individuals may have preauricular pits, lachrymal duct stenosis, hearing loss, branchial fistulas or cysts, structural defects of the outer, middle, and inner ear, and renal anomalies, which may range from mild hypoplasia to complete absence.
TextSentencer_T5 766-957 Sentence denotes Not all features of the syndrome are expressed in all carriers of the gene, but few carriers lack all the features, and the pits, branchial clefts, and hearing loss, are frequently expressed.
T5 766-957 Sentence denotes Not all features of the syndrome are expressed in all carriers of the gene, but few carriers lack all the features, and the pits, branchial clefts, and hearing loss, are frequently expressed.
TextSentencer_T6 958-1095 Sentence denotes Those offspring of affected persons who have pits or fistulas are likely (about 80%) to have hearing loss of varying degrees of severity.
T6 958-1095 Sentence denotes Those offspring of affected persons who have pits or fistulas are likely (about 80%) to have hearing loss of varying degrees of severity.
TextSentencer_T7 1096-1182 Sentence denotes A minority of heterozygotes (about 7%) may have hearing loss without pits or fistulas.
T7 1096-1182 Sentence denotes A minority of heterozygotes (about 7%) may have hearing loss without pits or fistulas.
TextSentencer_T8 1183-1244 Sentence denotes The risk of severe renal malformation is probably fairly low.
T8 1183-1244 Sentence denotes The risk of severe renal malformation is probably fairly low.
TextSentencer_T9 1245-1445 Sentence denotes Whether families that show dominant inheritance of pits, clefts, and deafness without renal anomalies represent variants of the BOR syndrome or a separate entity (the BO syndrome), is still not clear.
T9 1245-1445 Sentence denotes Whether families that show dominant inheritance of pits, clefts, and deafness without renal anomalies represent variants of the BOR syndrome or a separate entity (the BO syndrome), is still not clear.
TextSentencer_T10 1446-1564 Sentence denotes At present, any individual with preauricular pits and branchial clefts deserves both otologic and renal investigation.
T10 1446-1564 Sentence denotes At present, any individual with preauricular pits and branchial clefts deserves both otologic and renal investigation.