about
Analysis of possible genetic risk factors contributing to development of childhood acute lymphoblastic leukaemia in the Latvian population.Association between inherited monogenic liver disorders and chronic hepatitis C.Homocysteine and MTHFR C677T polymorphism in children and adolescents with psychotic and mood disorders.Association of ARID5B Genetic Variants with Risk of Childhood B Cell Precursor Acute Lymphoblastic Leukaemia in LatviaPerformance comparison of two whole genome amplification techniques in frame of multifactor preimplantation genetic testing.Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndromeNovel Variant of the Androgen Receptor Gene in a Patient With Complete Androgen Insensitivity Syndrome and PolyorchidismAssociation studies of candidate genes and cleft lip and palate taking into consideration geographical originVariation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palateInfluence of IL15 gene variations on the clinical features, treatment response and risk of developing childhood acute lymphoblastic leukemia in Latvian populationUGT1A1 Variants c.864+5G>T and c.996+2_996+5del of a Crigler-Najjar Patient Induce Aberrant Splicing in Minigene AssaysAllelic variants of breast cancer susceptibility genes PALB2 and RECQL in the Latvian populationAssociation of Variants in the CP, ATOX1 and COMMD1 Genes with Wilson Disease Symptoms in Latvia
P50
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P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Linda Piekuse
@en
Linda Piekuse
@nl
type
label
Linda Piekuse
@en
Linda Piekuse
@nl
prefLabel
Linda Piekuse
@en
Linda Piekuse
@nl
P31
P496
0000-0002-7219-1294