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https://olympias.lib.uoi.gr/jspui/handle/123456789/21348
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DC Field | Value | Language |
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dc.contributor.author | Syrrou, M. | en |
dc.contributor.author | Keymolen, K. | en |
dc.contributor.author | Devriendt, K. | en |
dc.contributor.author | Holvoet, M. | en |
dc.contributor.author | Thoelen, R. | en |
dc.contributor.author | Verhofstadt, K. | en |
dc.contributor.author | Fryns, J. P. | en |
dc.date.accessioned | 2015-11-24T19:14:36Z | - |
dc.date.available | 2015-11-24T19:14:36Z | - |
dc.identifier.issn | 0148-7299 | - |
dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/21348 | - |
dc.rights | Default Licence | - |
dc.subject | Chromosome Deletion | en |
dc.subject | Chromosomes, Human, Pair 2/genetics | en |
dc.subject | Family Health | en |
dc.subject | Female | en |
dc.subject | Fingers/*abnormalities | en |
dc.subject | Genetic Predisposition to Disease/*genetics | en |
dc.subject | Hand Deformities/complications/genetics | en |
dc.subject | Heparan Sulfate Proteoglycans/*genetics | en |
dc.subject | Humans | en |
dc.subject | In Situ Hybridization, Fluorescence | en |
dc.subject | Intellectual Disability/complications | en |
dc.subject | Male | en |
dc.subject | Middle Aged | en |
dc.title | Glypican 1 gene: good candidate for brachydactyly type E | en |
heal.type | journalArticle | - |
heal.type.en | Journal article | en |
heal.type.el | Άρθρο Περιοδικού | el |
heal.identifier.secondary | http://www.ncbi.nlm.nih.gov/pubmed/11920836 | - |
heal.identifier.secondary | http://onlinelibrary.wiley.com/store/10.1002/ajmg.10266/asset/10266_ftp.pdf?v=1&t=h0dilpfj&s=742e09964ac0e613fa28aba98a016169a996fe8a | - |
heal.language | en | - |
heal.access | campus | - |
heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικής | el |
heal.publicationDate | 2002 | - |
heal.abstract | In this report, we describe two siblings, a brother and a sister, with mental retardation and limb abnormalities (brachymetacarpy and brachymetatarsy in the brother and clinodactyly in his sister). Fluorescent in situ hybridization analysis (FISH) using subtelomeric probes proved that the patients carried an unbalanced subtelomeric rearrangement with 2qter deletion involving the Glypican 1 gene. Given the expression pattern in the developing limb bud, Glypican 1 gene represents a good candidate for brachydactyly E. | en |
heal.journalName | Am J Med Genet | en |
heal.journalType | peer-reviewed | - |
heal.fullTextAvailability | TRUE | - |
Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ |
Files in This Item:
File | Description | Size | Format | |
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Syrrou-2002-Glypican 1 gene_ goo.pdf | 217.53 kB | Adobe PDF | View/Open Request a copy |
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