Publications by authors named "Kati Kuuse"

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Enhanced proliferative capacity of human preadipocytes achieved by an optimized cultivating method that induces transient activity of hTERT.
Claudia G Cárdenas-León, Kristina Mäemets-Allas, Kati Kuuse, Luis A Salazar-Olivo, Viljar Jaks

Biochem Biophys Res Commun· August 2020

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Two familial microduplications of 15q26.3 causing overgrowth and variable intellectual disability with normal copy number of IGF1R.
Melanie Leffler, Sanna Puusepp, Olga Žilina, Ying Zhu, Kati Kuuse

Eur J Med Genet· April 2016

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The Diagnostic Utility of Single Long Contiguous Stretches of Homozygosity in Patients without Parental Consanguinity.
Sander Pajusalu, Olga Žilina, Maria Yakoreva, Pille Tammur, Kati Kuuse

Mol Syndromol· September 2015

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A patient with the classic features of Phelan-McDermid syndrome and a high immunoglobulin E level caused by a cryptic interstitial 0.72-Mb deletion in the 22q13.2 region.
Kristi Simenson, Eve Õiglane-Shlik, Rita Teek, Kati Kuuse, Katrin Õunap

Am J Med Genet A· March 2014

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Chromosomal microarray analysis as a first-tier clinical diagnostic test: Estonian experience.
Olga Zilina, Rita Teek, Pille Tammur, Kati Kuuse, Maria Yakoreva

Mol Genet Genomic Med· March 2014

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5.9 Mb microdeletion in chromosome band 17q22-q23.2 associated with tracheo-esophageal fistula and conductive hearing loss.
Helen Puusepp, Olga Zilina, Rita Teek, Katrin Männik, Sven Parkel, Kati Kuuse

Eur J Med Genet· April 2009

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