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Localization of the deleted segment in the cri-du-chat syndrome

✍ Scribed by E. Niebuhr

Publisher
Springer
Year
1972
Tongue
English
Weight
73 KB
Volume
16
Category
Article
ISSN
0340-6717

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Molecular cytogenetic and developmental assessment was performed on 50 individuals with cri-du-chat syndrome. Fluorescent in situ hybridization analysis was used to confirm a terminal deletion karyotype and map more precisely the location of the deletion breakpoint. We identified terminal deletion b