| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-110 |
Sentence |
denotes |
Molecular Karyotyping of a Dysmorphic Girl from Saudi Arabia with CYP1B1-negative Primary Congenital Glaucoma. |
| TextSentencer_T2 |
111-119 |
Sentence |
denotes |
PURPOSE: |
| TextSentencer_T3 |
120-379 |
Sentence |
denotes |
To report the results of molecular karyotyping for a dysmorphic girl with CYP1B1-negative primary congenital glaucoma from Saudi Arabia, where CYPB1 mutations account for over 90% of cases of primary congenital glaucoma and the remaining cases are idiopathic. |
| TextSentencer_T4 |
380-637 |
Sentence |
denotes |
METHODS: CYP1B1 sequencing in the affected child; high-resolution array comparative genomic hybridization (array CGH) of the affected child and both unaffected parents (Affymetrix Cytogenetics Whole-Genome 2.7M array; Affymetrix Inc., Santa Clara, CA, USA). |
| TextSentencer_T5 |
638-646 |
Sentence |
denotes |
RESULTS: |
| TextSentencer_T6 |
647-708 |
Sentence |
denotes |
The girl did not harbor CYP1B1 mutation by Sanger sequencing. |
| TextSentencer_T7 |
709-921 |
Sentence |
denotes |
Array CGH revealed 2 de novo 7p heterozygous duplications (7p21 - 7p14, encompassing 223 genes, and 7p14-7p11.2, encompassing 225 genes) and a 4p homozygous microdeletion (4p14) encompassing one gene only, DTHD1. |
| TextSentencer_T8 |
922-934 |
Sentence |
denotes |
CONCLUSIONS: |
| TextSentencer_T9 |
935-1124 |
Sentence |
denotes |
The fact that this dysmorphic girl is Saudi Arabian and has CYP1B1-negative primary congenital glaucoma suggests that her glaucoma phenotype is related to her de novo copy number variation. |
| TextSentencer_T10 |
1125-1307 |
Sentence |
denotes |
Loss or gain of one or more of the genes encompassed in the identified chromosomal areas may be associated with primary congenital glaucoma and/or other observed phenotypic features. |
| T1 |
0-110 |
Sentence |
denotes |
Molecular Karyotyping of a Dysmorphic Girl from Saudi Arabia with CYP1B1-negative Primary Congenital Glaucoma. |
| T2 |
111-119 |
Sentence |
denotes |
PURPOSE: |
| T3 |
120-379 |
Sentence |
denotes |
To report the results of molecular karyotyping for a dysmorphic girl with CYP1B1-negative primary congenital glaucoma from Saudi Arabia, where CYPB1 mutations account for over 90% of cases of primary congenital glaucoma and the remaining cases are idiopathic. |
| T4 |
380-637 |
Sentence |
denotes |
METHODS: CYP1B1 sequencing in the affected child; high-resolution array comparative genomic hybridization (array CGH) of the affected child and both unaffected parents (Affymetrix Cytogenetics Whole-Genome 2.7M array; Affymetrix Inc., Santa Clara, CA, USA). |
| T5 |
638-646 |
Sentence |
denotes |
RESULTS: |
| T6 |
647-708 |
Sentence |
denotes |
The girl did not harbor CYP1B1 mutation by Sanger sequencing. |
| T7 |
709-921 |
Sentence |
denotes |
Array CGH revealed 2 de novo 7p heterozygous duplications (7p21 - 7p14, encompassing 223 genes, and 7p14-7p11.2, encompassing 225 genes) and a 4p homozygous microdeletion (4p14) encompassing one gene only, DTHD1. |
| T8 |
922-934 |
Sentence |
denotes |
CONCLUSIONS: |
| T9 |
935-1124 |
Sentence |
denotes |
The fact that this dysmorphic girl is Saudi Arabian and has CYP1B1-negative primary congenital glaucoma suggests that her glaucoma phenotype is related to her de novo copy number variation. |
| T10 |
1125-1307 |
Sentence |
denotes |
Loss or gain of one or more of the genes encompassed in the identified chromosomal areas may be associated with primary congenital glaucoma and/or other observed phenotypic features. |