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Table 1 Primers used for qPCR in this study

From: The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability

Name

Primer sequence (5’ → 3’)

Forward

Reverse

chr1q21.1 #1

TGAGCAGTTCAAAGGAGTGTAG

ATGACCCACAAAGTGAGAGAAA

chr1q21.1 #2

AAGGCTGTGAAGGAGGAAATC

CTGACCAGGCAGAAGACATAAA

chr7q11

GGAGCACAAAGCAACTGAATG

AGACAGCAATGCAGAGGAA

chrXq28 #1

AGAGCTCGGACTCCATCTAAT

CCTTCCCATGTCAGTGTGTTAT

chrXq28 #2

CTCACTTCTGGGTCTCACATTC

AATCCCAAGTGACTTCCAAGG

GAPDH

GATCATCAGCAATGCCTCCT

ATGGCATGGACTGTGGTCAT

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Molecular Cytogenetics

ISSN: 1755-8166