2025-02-22T10:49:24-05:00 DEBUG: VuFindSearch\Backend\Solr\Connector: Query fl=%2A&wt=json&json.nl=arrarr&q=id%3A%22irk-123456789-126702%22&qt=morelikethis&rows=5
2025-02-22T10:49:24-05:00 DEBUG: VuFindSearch\Backend\Solr\Connector: => GET http://localhost:8983/solr/biblio/select?fl=%2A&wt=json&json.nl=arrarr&q=id%3A%22irk-123456789-126702%22&qt=morelikethis&rows=5
2025-02-22T10:49:24-05:00 DEBUG: VuFindSearch\Backend\Solr\Connector: <= 200 OK
2025-02-22T10:49:24-05:00 DEBUG: Deserialized SOLR response
Exclusion of chromosomal abnormalities and microdeletions 22q11 and 10p13 in Algerian patients with isolated conotruncal malformation
The chromosomal abnormalities of number and structure or the 22q11.2 and 10p13-14 microdeletions are considered the main causes of congenital heart disease. In our best knowledge, cytogenetics studies on congenital heart diseases (CHD) have not been performed in Algeria. In this study, we will scree...
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| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Інститут клітинної біології та генетичної інженерії НАН України
2015
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| Series: | Цитология и генетика |
| Subjects: | |
| Online Access: | http://dspace.nbuv.gov.ua/handle/123456789/126702 |
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