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List of works by Tiina Kahre

A descriptive epidemiological study of Duchenne muscular dystrophy in childhood in Estonia

scientific article

Aortic arch thrombosis in a neonate with heterozygous carrier status of factor V Leiden mutation

scientific article published on January 2006

Descriptive epidemiology of spinal muscular atrophy type I in Estonia

scientific article published in January 2006

Familial 1.3-Mb 11p15.5p15.4 Duplication in Three Generations Causing Silver-Russell and Beckwith-Wiedemann Syndromes

scientific article published on 24 July 2015

MODY2 caused by a novel mutation of GCK gene ⬇️

scientific article published on January 1, 2012

Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome.

scientific article

Presumed Perinatal Stroke: Risk Factors, Clinical and Radiological Findings.

scientific article published on 7 October 2015

Prevalence of Angelman syndrome and Prader-Willi syndrome in Estonian children: sister syndromes not equally represented.

scientific article

Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia

scientific article published on 18 June 2010

Prevalence of the fragile X syndrome among Estonian mentally retarded and the entire children's population

scientific article published in December 2008

Severe CF manifestation with anaemia and failure to thrive in a 394delTT homozygous patient.

scientific article

The Frequency of Methylation Abnormalities Among Estonian Patients Selected by Clinical Diagnostic Scoring Systems for Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome

scientific article

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