| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-108 |
Sentence |
denotes |
A de novo unbalanced reciprocal translocation identified as paternal in origin in the Prader-Willi syndrome. |
| T1 |
0-108 |
Sentence |
denotes |
A de novo unbalanced reciprocal translocation identified as paternal in origin in the Prader-Willi syndrome. |
| TextSentencer_T2 |
109-266 |
Sentence |
denotes |
Interstitial cytogenetic deletions involving the paternally derived chromosome 15q11-13 have been described in patients with the Prader-Willi syndrome (PWS). |
| T2 |
109-266 |
Sentence |
denotes |
Interstitial cytogenetic deletions involving the paternally derived chromosome 15q11-13 have been described in patients with the Prader-Willi syndrome (PWS). |
| TextSentencer_T3 |
267-367 |
Sentence |
denotes |
We report a child with PWS and a de novo unbalanced karyotype -45,XY,-9,-15,+der(9)t(9;15)(q34;q13). |
| T3 |
267-367 |
Sentence |
denotes |
We report a child with PWS and a de novo unbalanced karyotype -45,XY,-9,-15,+der(9)t(9;15)(q34;q13). |
| TextSentencer_T4 |
368-505 |
Sentence |
denotes |
Molecular studies with the DNA probe pML34 confirmed that only a single Prader Willi critical region (PWCR:15q11.2-q12) copy was present. |
| T4 |
368-505 |
Sentence |
denotes |
Molecular studies with the DNA probe pML34 confirmed that only a single Prader Willi critical region (PWCR:15q11.2-q12) copy was present. |
| TextSentencer_T5 |
506-689 |
Sentence |
denotes |
Hybridisation of patient and parental DNA with the multi-allelic probe CMW1, which maps to pter-15q13, showed that the chromosome involved in the translocation was paternal in origin. |
| T5 |
506-689 |
Sentence |
denotes |
Hybridisation of patient and parental DNA with the multi-allelic probe CMW1, which maps to pter-15q13, showed that the chromosome involved in the translocation was paternal in origin. |
| TextSentencer_T6 |
690-819 |
Sentence |
denotes |
This is the first example of a paternally-derived PWCR allele loss caused by an unbalanced translocation that has arisen de novo. |
| T6 |
690-819 |
Sentence |
denotes |
This is the first example of a paternally-derived PWCR allele loss caused by an unbalanced translocation that has arisen de novo. |