Konstantin Ridnõi

Konstantin Ridnõi

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Konstantin Ridnõi

Konstantin Ridnõi

Publications by authors named "Konstantin Ridnõi"

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1PubMed Central Citations

A prenatally diagnosed case of Meckel-Gruber syndrome with novel compound heterozygous pathogenic variants in the TXNDC15 gene.

Authors:
Konstantin Ridnõi Marek Šois Eve Vaidla Sander Pajusalu Larissa Kelder Tiia Reimand Katrin Õunap

Mol Genet Genomic Med 2019 05 9;7(5):e614. Epub 2019 Mar 9.

Department of Clinical Genetics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.

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http://dx.doi.org/10.1002/mgg3.614DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503012PMC
May 2019

Two Consecutive Pregnancies with Simpson-Golabi-Behmel Syndrome Type 1: Case Report and Review of Published Prenatal Cases.

Authors:
Konstantin Ridnõi Elvira Kurvinen Sander Pajusalu Tiia Reimand Katrin Õunap

Mol Syndromol 2018 Jul 8;9(4):205-213. Epub 2018 Jun 8.

Department of Clinical Genetics, Institute of Clinical Medicine.

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http://dx.doi.org/10.1159/000490083DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6108232PMC
July 2018