| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-98 |
Sentence |
denotes |
Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosis. |
| T1 |
0-98 |
Sentence |
denotes |
Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosis. |
| TextSentencer_T2 |
99-269 |
Sentence |
denotes |
We have performed linkage analysis with the DNA markers DXS52 and the clotting factor VIII gene (F8C), in several large families with X-linked adrenoleukodystrophy (ALD). |
| T2 |
99-269 |
Sentence |
denotes |
We have performed linkage analysis with the DNA markers DXS52 and the clotting factor VIII gene (F8C), in several large families with X-linked adrenoleukodystrophy (ALD). |
| TextSentencer_T3 |
270-358 |
Sentence |
denotes |
The tight linkage to DXS52 could be extended giving a maximal LOD score of 22.5 at 1 cM. |
| T3 |
270-358 |
Sentence |
denotes |
The tight linkage to DXS52 could be extended giving a maximal LOD score of 22.5 at 1 cM. |
| TextSentencer_T4 |
359-448 |
Sentence |
denotes |
F8C was also tightly linked to ALD with a maximal LOD score of 7.8 without recombination. |
| T4 |
359-448 |
Sentence |
denotes |
F8C was also tightly linked to ALD with a maximal LOD score of 7.8 without recombination. |
| TextSentencer_T5 |
449-586 |
Sentence |
denotes |
Multipoint linkage analysis with the markers DXS304, DXS52, and F8C indicated that both the gene for ALD and for F8C are distal to DXS52. |
| T5 |
449-586 |
Sentence |
denotes |
Multipoint linkage analysis with the markers DXS304, DXS52, and F8C indicated that both the gene for ALD and for F8C are distal to DXS52. |
| TextSentencer_T6 |
587-755 |
Sentence |
denotes |
In four patients with ALD, no major structural rearrangement in the Xqter region was observed; in particular, there were no abnormalities in the vision blindness genes. |
| T6 |
587-755 |
Sentence |
denotes |
In four patients with ALD, no major structural rearrangement in the Xqter region was observed; in particular, there were no abnormalities in the vision blindness genes. |
| TextSentencer_T7 |
756-953 |
Sentence |
denotes |
DNA analysis appeared to be of use in determination of the carrier status of females at risk, for the determination of the origin of the mutation in a particular family, and for prenatal diagnosis. |
| T7 |
756-953 |
Sentence |
denotes |
DNA analysis appeared to be of use in determination of the carrier status of females at risk, for the determination of the origin of the mutation in a particular family, and for prenatal diagnosis. |