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Fig. 3 | Human Genomics

Fig. 3

From: Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree

Fig. 3

ROH and identification of KALRN. The dark blue areas demarcate the positions of the genome that are homozygous and respect the familial segregation. The horizontal red line shows the position of KALRN in chromosome 3. Gray areas designate the small arms of the acrocentric chromosomes and known heterochromatic areas (figure made through http://db.systemsbiology.net/gestalt/cgi-pub/genomeMapBlocks.pl)

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Human Genomics

ISSN: 1479-7364