Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-138 |
Sentence |
denotes |
Investigation of three patients with the "ring syndrome", including familial transmission of ring 5, and estimation of reproductive risks. |
TextSentencer_T2 |
139-242 |
Sentence |
denotes |
We report three cases of ring chromosome 5 [r(5)], two familial (mother and daughter) and one sporadic. |
TextSentencer_T3 |
243-412 |
Sentence |
denotes |
The phenotype resembled that of the "ring syndrome" with prenatal onset of short stature, growth retardation, mild facial dysmorphism and normal psychomotor development. |
TextSentencer_T4 |
413-584 |
Sentence |
denotes |
Extended metaphase and prometaphase chromosome preparations using G-, R- and Q-banding and scanning electron microscopy (SEM) failed to demonstrate deletion in the ring 5. |
TextSentencer_T5 |
585-720 |
Sentence |
denotes |
Flow karyotype using the FACS cell sorter and peak area analysis showed the r(5) to be in the same position as the normal chromosome 5. |
TextSentencer_T6 |
721-833 |
Sentence |
denotes |
The deletion that is presumably associated with ring formation appears to involve less that one megabase of DNA. |
TextSentencer_T7 |
834-964 |
Sentence |
denotes |
In the "complex" rings, high resolution SEM showed fragile sites at the 5q34 and 5q35 region with frequent deletions at that site. |
TextSentencer_T8 |
965-1096 |
Sentence |
denotes |
A literature survey suggests that when a parent carries a ring chromosome about 80% of recognised pregnancies result in live birth. |
TextSentencer_T9 |
1097-1274 |
Sentence |
denotes |
Of these, about half have a normal phenotype and karyotype, and half inherit the parental ring; about half of those acquiring the ring (20%) show significant mental retardation. |
T1 |
0-138 |
Sentence |
denotes |
Investigation of three patients with the "ring syndrome", including familial transmission of ring 5, and estimation of reproductive risks. |
T2 |
139-242 |
Sentence |
denotes |
We report three cases of ring chromosome 5 [r(5)], two familial (mother and daughter) and one sporadic. |
T3 |
243-412 |
Sentence |
denotes |
The phenotype resembled that of the "ring syndrome" with prenatal onset of short stature, growth retardation, mild facial dysmorphism and normal psychomotor development. |
T4 |
413-584 |
Sentence |
denotes |
Extended metaphase and prometaphase chromosome preparations using G-, R- and Q-banding and scanning electron microscopy (SEM) failed to demonstrate deletion in the ring 5. |
T5 |
585-720 |
Sentence |
denotes |
Flow karyotype using the FACS cell sorter and peak area analysis showed the r(5) to be in the same position as the normal chromosome 5. |
T6 |
721-833 |
Sentence |
denotes |
The deletion that is presumably associated with ring formation appears to involve less that one megabase of DNA. |
T7 |
834-964 |
Sentence |
denotes |
In the "complex" rings, high resolution SEM showed fragile sites at the 5q34 and 5q35 region with frequent deletions at that site. |
T8 |
965-1096 |
Sentence |
denotes |
A literature survey suggests that when a parent carries a ring chromosome about 80% of recognised pregnancies result in live birth. |
T9 |
1097-1274 |
Sentence |
denotes |
Of these, about half have a normal phenotype and karyotype, and half inherit the parental ring; about half of those acquiring the ring (20%) show significant mental retardation. |