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"name": "GM12561 cell",
"definition": "[' CEPH/FRENCH PEDIGREE 12']",
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{
"accession": "CLO:0017765",
"name": "GM12562 cell",
"definition": "[' CEPH/FRENCH PEDIGREE 12']",
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"name": "GM12563 cell",
"definition": "[' CEPH/FRENCH PEDIGREE 12']",
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{
"accession": "CLO:0017767",
"name": "GM12564 cell",
"definition": "[' CEPH/FRENCH PEDIGREE 12']",
"term_type": "cell line"
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{
"accession": "CLO:0017768",
"name": "GM12565 cell",
"definition": "[' CEPH/FRENCH PEDIGREE 12']",
"term_type": "cell line"
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{
"accession": "CLO:0017769",
"name": "GM12566 cell",
"definition": "[' CEPH/FRENCH PEDIGREE 12']",
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{
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"name": "GM12567 cell",
"definition": "[' CEPH/FRENCH PEDIGREE 12']",
"term_type": "cell line"
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{
"accession": "CLO:0018116",
"name": "GM12568 cell",
"definition": "[' CEPH/FRENCH PEDIGREE 12']",
"term_type": "cell line"
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{
"accession": "CLO:0018109",
"name": "GM12569 cell",
"definition": "[' CEPH/FRENCH PEDIGREE 12']",
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{
"accession": "CLO:0018107",
"name": "GM12570 cell",
"definition": "[' CEPH/FRENCH PEDIGREE 12']",
"term_type": "cell line"
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{
"accession": "CLO:0018114",
"name": "GM12571 cell",
"definition": "[' CEPH/FRENCH PEDIGREE 12']",
"term_type": "cell line"
},
{
"accession": "CLO:0018111",
"name": "GM12572 cell",
"definition": "[' CEPH/FRENCH PEDIGREE 12']",
"term_type": "cell line"
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{
"accession": "CLO:0018094",
"name": "GM12573 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
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{
"accession": "CLO:0018095",
"name": "GM12583 cell",
"definition": "[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']",
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{
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"name": "GM12585 cell",
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"term_type": "cell line"
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{
"accession": "CLO:0018092",
"name": "GM12592 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
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{
"accession": "CLO:0018080",
"name": "GM12593 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0018079",
"name": "GM12601 cell",
"definition": "[' HYPOPLASTIC LEFT HEART SYNDROME']",
"term_type": "cell line"
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{
"accession": "CLO:0018077",
"name": "GM12604 cell",
"definition": "[' ORNITHINE CARBAMOYLTRANSFERASE; OTC ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO; OTC']",
"term_type": "cell line"
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{
"accession": "CLO:0018088",
"name": "GM12606 cell",
"definition": "[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC CHROMOSOME DELETION']",
"term_type": "cell line"
}
]
}