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Search Results - Ridnõi, Konstantin
Search Results - Ridnõi, Konstantin
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Two Consecutive Pregnancies with Simpson-Golabi-Behmel Syndrome Type 1: Case Report and Review of Published Prenatal Cases
by
Ridnõi, Konstantin
,
Kurvinen, Elvira
,
Pajusalu, Sander
,
Reimand, Tiia
,
Õunap, Katrin
Published in
Molecular syndromology
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A prenatally diagnosed case of Meckel–Gruber syndrome with novel compound heterozygous pathogenic variants in the TXNDC15 gene
by
Ridnõi, Konstantin
,
Šois, Marek
,
Vaidla, Eve
,
Pajusalu, Sander
,
Kelder, Larissa
,
Reimand, Tiia
,
Õunap, Katrin
Published in
Molecular genetics & genomic medicine
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A two‐year prospective study assessing the performance of fetal chromosomal microarray analysis and next‐generation sequencing in high‐risk pregnancies
by
Ridnõi, Konstantin
,
Muru, Kai
,
Keernik, Maria
,
Pajusalu, Sander
,
Ustav, Eva‐Liina
,
Tammur, Pille
,
Mölter‐Väär, Triin
,
Kahre, Tiina
,
Šamarina, Ustina
,
Asser, Karin
,
Szirko, Ferenc
,
Reimand, Tiia
,
Õunap, Katrin
Published in
Molecular genetics & genomic medicine
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Creating basis for introducing non‐invasive prenatal testing in the Estonian public health setting
by
Žilina, Olga
,
Rekker, Kadri
,
Kaplinski, Lauris
,
Sauk, Martin
,
Paluoja, Priit
,
Teder, Hindrek
,
Ustav, Eva‐Liina
,
Tõnisson, Neeme
,
Reimand, Tiia
,
Ridnõi, Konstantin
,
Palta, Priit
,
Vermeesch, Joris Robert
,
Krjutškov, Kaarel
,
Kurg, Ants
,
Salumets, Andres
Published in
Prenatal diagnosis
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Prenatal diagnosis
by
Žilina, Olga
,
Rekker, Kadri
,
Kaplinski, Lauris
,
Sauk, Martin
,
Paluoja, Priit
,
Teder, Hindrek
,
Ustav, Eva-Liina
,
Tõnisson, Neeme
,
Reimand, Tiia
,
Ridnõi, Konstantin
,
Palta, Priit
,
Vermeesch, Joris Robert
,
Krjutškov, Kaarel
,
Kurg, Ants
,
Salumets, Andres
Published in
Prenatal diagnosis
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Molecular Genetics & Genomic Medicine
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Prenatal Diagnosis
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Molecular Syndromology
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Genetics & Heredity
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Life Sciences & Biomedicine
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Science & Technology
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Fetuses
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Ultrasound
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Genetic Disorders
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Genomes
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Ciliary Motility Disorders - Diagnosis
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