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Publications by Eglė Preikšaitienė

A Case Report of Familial 4q13.3 Microdeletion in Three Individuals With Syndromic Intellectual Disability

BMC Medical Genomics
Genetics
2020English

De Novo Splice Site Variant of ARID1B Associated With Pathogenesis of Coffin–Siris Syndrome

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2019English

Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient With Androgen Insensitivity Syndrome

Journal of Pediatric and Adolescent Gynecology
Child HealthGynecologyPerinatologyObstetricsMedicinePediatrics
2019English

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