Rare human diseases: 9p deletion syndrome
Objective of the study was to review the anamnesis, pheno - and genotype in patients with rare chromosome disorders such as 9p deletion syndrome. Genetic methods of investigation (clinical and genealogical, cytogenetic, FISH- method), paraclinical and instrumental methods of examination were used. K...
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| Format: | Article |
| Language: | English |
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SE "Dnipropetrovsk medical academy of Health Ministry of Ukraine"
2014-09-01
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| Series: | Medičnì Perspektivi |
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| Online Access: | http://medpers.dsma.dp.ua/issues/2014/N3/15-18.pdf |