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PubMed:657583 JSONTXT 9 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-99 Sentence denotes Branchio-oto-renal dysplasia and branchio-oto dysplasia: two distinct autosomal dominant disorders.
T1 0-99 Sentence denotes Branchio-oto-renal dysplasia and branchio-oto dysplasia: two distinct autosomal dominant disorders.
TextSentencer_T2 100-215 Sentence denotes Three families are presented, one with branchio-oto-renal dysplasia (BOR) and two with branchio-oto dysplasia (BO).
T2 100-215 Sentence denotes Three families are presented, one with branchio-oto-renal dysplasia (BOR) and two with branchio-oto dysplasia (BO).
TextSentencer_T3 216-362 Sentence denotes The former syndrome is characterized by external ear malformations, cervical fistulae, mixed hearing loss and renal anomalies of varying severity.
T3 216-362 Sentence denotes The former syndrome is characterized by external ear malformations, cervical fistulae, mixed hearing loss and renal anomalies of varying severity.
TextSentencer_T4 363-499 Sentence denotes The latter syndrome differs in that there are no renal anomalies and that the sensorineural component of the hearing loss may be absent.
T4 363-499 Sentence denotes The latter syndrome differs in that there are no renal anomalies and that the sensorineural component of the hearing loss may be absent.
TextSentencer_T5 500-568 Sentence denotes The external ear malformations are quite variable in both syndromes.
T5 500-568 Sentence denotes The external ear malformations are quite variable in both syndromes.
TextSentencer_T6 569-738 Sentence denotes Evidence is presented which supports the idea that these two syndromes are not phenotypic variants of the same autosomal dominant mutation but distinct disease entities.
T6 569-738 Sentence denotes Evidence is presented which supports the idea that these two syndromes are not phenotypic variants of the same autosomal dominant mutation but distinct disease entities.
TextSentencer_T7 739-1073 Sentence denotes The BOR syndrome appears to belong to a larger group of hereditary ear dysplasia-renal adysplasia syndromes that must be carefully ruled out in all patients with familial branchial arch malformations as well as in the parents and siblings of infants with "Potter facies" in the presence of auricular malformation and renal adysplasia.
T7 739-1073 Sentence denotes The BOR syndrome appears to belong to a larger group of hereditary ear dysplasia-renal adysplasia syndromes that must be carefully ruled out in all patients with familial branchial arch malformations as well as in the parents and siblings of infants with "Potter facies" in the presence of auricular malformation and renal adysplasia.