Data di Pubblicazione:
2005
Abstract:
We report on a 5p- azoospermic male not showing the clinical features diagnostic for the cri-du-chat syndrome but for a breathy, raspy voice. The 5p deletion breakpoint, determined by fluorescent in situ hybridization (FISH) analysis with BAC clones, maps 8.5 Mb far from the short arm telomere in 5p15.31. Genotype/phenotype correlations in this subject, including his neuropsychological assessment, led us to define that the gene for the cat-like cry and one gene responsible for mild mental retardation with speech delay map both in the distal 8.5 Mb of chromosome 5 short arm
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
"DELETION"; "ARRAY CGH"; "AZOOSPERMIA"
Elenco autori:
Rossi, Elena; DE GREGORI, M.; GRAZIA PATRICELLI, M.; Pramparo, T.; Argentiero, L.; Giglio, S.; Sosta, K.; Foresti, G.; Zuffardi, Orsetta
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