Anna Jarmolowicz

3PUBLICATIONS
5CO-AUTHORS
Child language acquisitionGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)
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Publications (3)

|Sep 15, 2023
An Investigation of Barriers and Enablers for Genetics in Speech-Language Pathology Explored Through a Case Study of Childhood Apraxia of Speech.

Mariana L Lauretta, Anna Jarmolowicz, David J Amor

|Jun 29, 2021
Personal utility of genomic sequencing for infants with congenital deafness.

Erin Tutty, David J Amor, Anna Jarmolowicz

|Feb 05, 2021
Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program.

Anna I Jarmolowicz, Emma K Baker, Essra Bartlett

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