Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-115 |
Sentence |
denotes |
A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type. |
T1 |
0-115 |
Sentence |
denotes |
A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type. |
TextSentencer_T2 |
116-239 |
Sentence |
denotes |
Two siblings with a short-limb dwarfing condition which we call acromesomelic dysplasia, Hunter-Thompson type are reported. |
T2 |
116-239 |
Sentence |
denotes |
Two siblings with a short-limb dwarfing condition which we call acromesomelic dysplasia, Hunter-Thompson type are reported. |
TextSentencer_T3 |
240-327 |
Sentence |
denotes |
Abnormalities are limited to the limbs and limb joints in this severe form of dwarfism. |
T3 |
240-327 |
Sentence |
denotes |
Abnormalities are limited to the limbs and limb joints in this severe form of dwarfism. |
TextSentencer_T4 |
328-390 |
Sentence |
denotes |
The middle and distal segments of the limbs are most affected. |
T4 |
328-390 |
Sentence |
denotes |
The middle and distal segments of the limbs are most affected. |
TextSentencer_T5 |
391-440 |
Sentence |
denotes |
The lower limbs are more affected than the upper. |
T5 |
391-440 |
Sentence |
denotes |
The lower limbs are more affected than the upper. |
TextSentencer_T6 |
441-516 |
Sentence |
denotes |
We are aware of one previously published case of this entity reported by A. |
T6 |
441-516 |
Sentence |
denotes |
We are aware of one previously published case of this entity reported by A. |
TextSentencer_T7 |
517-519 |
Sentence |
denotes |
G. |
T7 |
517-519 |
Sentence |
denotes |
G. |
TextSentencer_T8 |
520-522 |
Sentence |
denotes |
W. |
T8 |
520-522 |
Sentence |
denotes |
W. |
TextSentencer_T9 |
523-536 |
Sentence |
denotes |
Hunter and M. |
T9 |
523-536 |
Sentence |
denotes |
Hunter and M. |
TextSentencer_T10 |
537-539 |
Sentence |
denotes |
W. |
T10 |
537-539 |
Sentence |
denotes |
W. |
TextSentencer_T11 |
540-557 |
Sentence |
denotes |
Thompson in 1976. |
T11 |
540-557 |
Sentence |
denotes |
Thompson in 1976. |
TextSentencer_T12 |
558-677 |
Sentence |
denotes |
Dislocations of the elbows and ankles were present in all three patients and dislocations of the hips and knees in two. |
T12 |
558-677 |
Sentence |
denotes |
Dislocations of the elbows and ankles were present in all three patients and dislocations of the hips and knees in two. |
TextSentencer_T13 |
678-834 |
Sentence |
denotes |
One of the siblings who did not have hip and knee dislocations clinically resembled Grebe chondrodysplasia, another severe acromesomelic dwarfing condition. |
T13 |
678-834 |
Sentence |
denotes |
One of the siblings who did not have hip and knee dislocations clinically resembled Grebe chondrodysplasia, another severe acromesomelic dwarfing condition. |
TextSentencer_T14 |
835-995 |
Sentence |
denotes |
However, radiological analysis suggests that while acromesomelic dysplasia, Hunter-Thompson type and Grebe chondrodysplasia are related, they are not identical. |
T14 |
835-995 |
Sentence |
denotes |
However, radiological analysis suggests that while acromesomelic dysplasia, Hunter-Thompson type and Grebe chondrodysplasia are related, they are not identical. |
TextSentencer_T15 |
996-1072 |
Sentence |
denotes |
Grebe chondrodysplasia has been established as an autosomal recessive trait. |
T15 |
996-1072 |
Sentence |
denotes |
Grebe chondrodysplasia has been established as an autosomal recessive trait. |
TextSentencer_T16 |
1073-1163 |
Sentence |
denotes |
It appears probable that the entity we describe has the same mode of genetic transmission. |
T16 |
1073-1163 |
Sentence |
denotes |
It appears probable that the entity we describe has the same mode of genetic transmission. |