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PubMed:2227937 JSONTXT

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sentences

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.

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 318-331 HP_0004322 denotes short stature
T2 333-351 HP_0001510 denotes growth retardation
T3 358-376 HP_0001999 denotes facial dysmorphism
T4 1255-1273 HP_0001249 denotes mental retardation

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 318-331 HP:0004322 denotes short stature

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 164-181 ORDO:251043 denotes ring chromosome 5