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PubMed:6214946 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-109 Sentence denotes A five-generation family with sacral agenesis and spina bifida: possible similarities with the mouse T-locus.
TextSentencer_T2 110-226 Sentence denotes In man, a malformation that recalls some of the defects associated with T/t mutants in the mouse is sacral agenesis.
TextSentencer_T3 227-453 Sentence denotes We report on a family with a high incidence of sacral malformation, ranging from a complete absence of the sacrum (SA), with or without spina bifida aperta, to a spina bifida occulta (SBO) that could only be detected by x-ray.
TextSentencer_T4 454-590 Sentence denotes The condition appeared in a man with four children who were all affect, and thereafter, to varying degrees, in 17 of his 28 descendants.
TextSentencer_T5 591-714 Sentence denotes Segregation analysis has been performed in this family, using the Elston and Stewart transmission probability model [1971].
TextSentencer_T6 715-790 Sentence denotes The two traits (SA and SBO) were first studied separated and then together.
TextSentencer_T7 791-849 Sentence denotes A fully penetrant major dominant gene is show to cause SA.
TextSentencer_T8 850-941 Sentence denotes When the phenotypes SA and SBO are considered together, Mendelian transmission is rejected.
TextSentencer_T9 942-1191 Sentence denotes This could be explained genetically by two alternative hypotheses: genetic heterogeneity or a dominant major gene transmitted in excess by heterozygotes (tau Aa A = 0.896), suggesting a segregation distortion property of an allele at a T-like locus.
T1 0-109 Sentence denotes A five-generation family with sacral agenesis and spina bifida: possible similarities with the mouse T-locus.
T2 110-226 Sentence denotes In man, a malformation that recalls some of the defects associated with T/t mutants in the mouse is sacral agenesis.
T3 227-453 Sentence denotes We report on a family with a high incidence of sacral malformation, ranging from a complete absence of the sacrum (SA), with or without spina bifida aperta, to a spina bifida occulta (SBO) that could only be detected by x-ray.
T4 454-590 Sentence denotes The condition appeared in a man with four children who were all affect, and thereafter, to varying degrees, in 17 of his 28 descendants.
T5 591-714 Sentence denotes Segregation analysis has been performed in this family, using the Elston and Stewart transmission probability model [1971].
T6 715-790 Sentence denotes The two traits (SA and SBO) were first studied separated and then together.
T7 791-849 Sentence denotes A fully penetrant major dominant gene is show to cause SA.
T8 850-941 Sentence denotes When the phenotypes SA and SBO are considered together, Mendelian transmission is rejected.
T9 942-1191 Sentence denotes This could be explained genetically by two alternative hypotheses: genetic heterogeneity or a dominant major gene transmitted in excess by heterozygotes (tau Aa A = 0.896), suggesting a segregation distortion property of an allele at a T-like locus.

PubCasesHPO

Id Subject Object Predicate Lexical cue
TI1 50-62 HP:0002414 denotes spina bifida
AB1 319-340 HP:0010305 denotes absence of the sacrum
AB2 363-375 HP:0002414 denotes spina bifida
AB3 389-409 HP:0003298 denotes spina bifida occulta

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 363-382 ORDO:268369 denotes spina bifida aperta