The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2.

The 18q- syndrome is one of several terminal deletion disorders that occur in humans. Previous G-banding studies suggest that the loss of a critical band, 18q21.3, results in mental retardation, craniofacial anomalies, and metabolic defects. However, it is difficult to reconcile the consistent loss...

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Tallennettuna:
Bibliografiset tiedot
Päätekijät: Silverman, G A, Schneider, S S, Massa, H F, Flint, A, Lalande, M, Leonard, J C, Overhauser, J, van den Engh, G, Trask, B J
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1995
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801205/
https://ncbi.nlm.nih.gov/pubmed/7717403
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