Implication of Genetic Testing and Pregnancy Outcome in a Woman with Unbalanced Translocation t(1;6)

por Jurčenko, Marija, Auzenbaha, Madara, Mičule, Ieva, Grīnfelde, Ieva, Dzalbs, Aigars, Mālniece, Ieva
Publicado 2022

The Fetal Phenotype of Noonan Syndrome Caused by Severe, Cancer-Related PTPN11 Variants

por Malniece, Ieva, Grasmane, Adele, Inashkina, Inna, Stavusis, Janis, Kreile, Madara, Miklasevics, Edvins, Gailite, Linda
Publicado 2020

The First Registered Type 0 Spinal Muscular Atrophy Patient in Latvia: Call for Change in Prenatal Diagnostic Procedures

por Čupāne, Tīna Luīze, Dīriks, Mikus, Tauriņa, Gita, Korņejeva, Liene, Gailīte, Linda, Mālniece, Ieva, Auzenbaha, Madara
Publicado 2023

Two Cases of Leigh Syndrome in One Family: Diagnostic Challenges and Clinical Management Experience in Latvia

por Katkevica, Arta, Kreile, Madara, Grinfelde, Ieva, Taurina, Gita, Micule, Ieva, Dzivite-Krisane, Iveta, Smite-Laguna, Arta, Malniece, Ieva
Publicado 2021

Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of Latvia

por Lace, Baiba, Micule, Ieva, Kenina, Viktorija, Setlere, Signe, Strautmanis, Jurgis, Kazaine, Inese, Taurina, Gita, Murmane, Daiga, Grinfelde, Ieva, Kornejeva, Liene, Krumina, Zita, Sterna, Olga, Radovica-Spalvina, Ilze, Vasiljeva, Inta, Gailite, Linda, Stavusis, Janis, Livcane, Diana, Kidere, Dita, Malniece, Ieva, Inashkina, Inna
Publicado 2022