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Chromosome 17, trisomy 17p
, Trisomy 17p
National Institutes of Health
Chromosome 17p Deletion Syndrome
Chromosomes, Human, Pair 17
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Molecular characterization of near-complete trisomy 17p syndrome from inverted duplication in association with cryptic deletion of 17pter.
Corpus ID: 205019182
Trisomy of the short arm of chromosome 17 (T17P) is a genomic disorder presenting with growth retardation, motor and mental…
Trisomy 17p due to A t(5;17) (p15;p11) pat translocation.
Annales de genetique
Corpus ID: 40714091
A 6-month-old Japanese boy with trisomy 17p, resulting from a paternal balanced translocation t(5;17)(p15;p11), is described…
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