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Chriselle Hickerton

Showing results (11-20 of 16) with videos related to

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Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|February 26, 2021
The expectations and realities of nutrigenomic testing in australia: A qualitative studyErin Tutty, Chriselle Hickerton, Bronwyn Terrill, et al.
European Journal of Medical Genetics|November 16, 2018
Australians' perspectives on support around use of personal genomic testing: Findings from the Genioz studySylvia A Metcalfe, Chriselle Hickerton, Jacqueline Savard, et al.
International Journal of Molecular Sciences|August 14, 2019
Significantly Elevated <i>FMR1</i> mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X TestingMichael Field, Tracy Dudding-Byth, Marta Arpone, et al.
European Journal of Human Genetics : EJHG|January 12, 2012
ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasibleMartin B Delatycki, Michelle Wolthuizen, Veronica Collins, et al.
Scientific Reports|February 28, 2018
Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile XMarta Arpone, Emma K Baker, Lesley Bretherton, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2017
Informed decision making and psychosocial outcomes in pregnant and nonpregnant women offered population fragile X carrier screeningSylvia A Metcalfe, Melissa Martyn, Alice Ames, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|February 26, 2021
The expectations and realities of nutrigenomic testing in australia: A qualitative studyErin Tutty, Chriselle Hickerton, Bronwyn Terrill, et al.
European Journal of Medical Genetics|November 16, 2018
Australians' perspectives on support around use of personal genomic testing: Findings from the Genioz studySylvia A Metcalfe, Chriselle Hickerton, Jacqueline Savard, et al.
International Journal of Molecular Sciences|August 14, 2019
Significantly Elevated <i>FMR1</i> mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X TestingMichael Field, Tracy Dudding-Byth, Marta Arpone, et al.
European Journal of Human Genetics : EJHG|January 12, 2012
ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasibleMartin B Delatycki, Michelle Wolthuizen, Veronica Collins, et al.
Scientific Reports|February 28, 2018
Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile XMarta Arpone, Emma K Baker, Lesley Bretherton, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2017
Informed decision making and psychosocial outcomes in pregnant and nonpregnant women offered population fragile X carrier screeningSylvia A Metcalfe, Melissa Martyn, Alice Ames, et al.
Pageof 2