| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-90 |
Sentence |
denotes |
Constitutional translocation t(4;22) (q12;q12.2) associated with neurofibromatosis type 2. |
| TextSentencer_T2 |
91-293 |
Sentence |
denotes |
We report on a female patient with bilateral acoustic neurinomas and other tumors in the central nervous system (neurofibromatosis type 2: NF2) and the constitutional translocation, t(4;22) (q12;q12.2). |
| TextSentencer_T3 |
294-534 |
Sentence |
denotes |
The precise identification of the translocation breakpoint (q12.2) on chromosome 22 implies the refined localization of a gene responsible for NF2, and would provide a clue to its molecular characterization and to the isolation of the gene. |
| TextSentencer_T4 |
535-686 |
Sentence |
denotes |
Chromosomes of a paraspinal neurinoma from the patient were also analyzed, and the same karyotype as seen in cultured peripheral lymphocytes was found. |
| TextSentencer_T5 |
687-813 |
Sentence |
denotes |
The patient's father was also a carrier of the translocation, but he had no clinical symptoms of NF2, nor did other relatives. |
| TextSentencer_T6 |
814-932 |
Sentence |
denotes |
Several explanations are offered for the different expression of the translocation between the patient and her father. |
| T1 |
0-90 |
Sentence |
denotes |
Constitutional translocation t(4;22) (q12;q12.2) associated with neurofibromatosis type 2. |
| T2 |
91-293 |
Sentence |
denotes |
We report on a female patient with bilateral acoustic neurinomas and other tumors in the central nervous system (neurofibromatosis type 2: NF2) and the constitutional translocation, t(4;22) (q12;q12.2). |
| T3 |
294-534 |
Sentence |
denotes |
The precise identification of the translocation breakpoint (q12.2) on chromosome 22 implies the refined localization of a gene responsible for NF2, and would provide a clue to its molecular characterization and to the isolation of the gene. |
| T4 |
535-686 |
Sentence |
denotes |
Chromosomes of a paraspinal neurinoma from the patient were also analyzed, and the same karyotype as seen in cultured peripheral lymphocytes was found. |
| T5 |
687-813 |
Sentence |
denotes |
The patient's father was also a carrier of the translocation, but he had no clinical symptoms of NF2, nor did other relatives. |
| T6 |
814-932 |
Sentence |
denotes |
Several explanations are offered for the different expression of the translocation between the patient and her father. |