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Pressure Palsy, deletion c'some 17, cosmid

Pressure palsy, deletion c'some 17, cosmid

Human chromosomes from a patient with Hereditary
Liability to Pressure Palsy (a lesion of a spinal
root or peripheral nerve resulting from
compression). There is a deletion in chromosome 17
(17p11.2), which has been highlighted using a
fluorescent cosmid probe (red) from the PMP gene.
The chromosome 11 centromeres are green. The
chromosomes have been highlighted with fluorescent
probes that bind to specific sequences of DNA.
Image by Dr John Crolla.

Human chromosomes from a patient with Hereditary
Liability to Pressure Palsy. The chromosomes have
been highlighted with fluorescent probes that bind
to specific sequences of DNA. There is a deletion
in chromosome 17 (see B0000306C). The chromosome
17 telomeres are green. A control cosmid probe
(red) outside the PMP gene region is not deleted.
Pressure palsy is a lesion of a spinal root or
peripheral nerve resulting in from compression.
Image by Dr John Crolla.

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PRESSURE PALSY

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Pressure palsy, deletion c'some 17, cosmid

Pressure Palsy, deletion c'some 17, cosmid

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PRESSURE PALSY

Images

Catalogue

Pressure palsy, deletion c'some 17, cosmid

Pressure Palsy, deletion c'some 17, cosmid

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