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Evidence-Based Complementary and Alternative Medicine : Ecam
|
June 22, 2012
Epigenetic changes in response to tai chi practice: a pilot investigation of DNA methylation marks
Hua Ren, Veronica Collins, Sandy J Clarke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 27, 2008
A model for offering carrier screening for fragile X syndrome to nonpregnant women: results from a pilot study
Sylvia Metcalfe, Alice Jacques, Alison Archibald, et al.
Orphanet Journal of Rare Diseases
|
November 12, 2022
Clinical management guidelines for Friedreich ataxia: best practice in rare diseases
Louise A Corben, Veronica Collins, Sarah Milne, et al.
Brain : a Journal of Neurology
|
February 2, 2008
Vestibular, saccadic and fixation abnormalities in genetically confirmed Friedreich ataxia
Michael C Fahey, Phillip D Cremer, Swee T Aw, et al.
European Journal of Human Genetics : EJHG
|
January 12, 2012
ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible
Martin B Delatycki, Michelle Wolthuizen, Veronica Collins, et al.
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Search research articles
Search
Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 25 results.
Evidence-Based Complementary and Alternative Medicine : Ecam
|
June 22, 2012
Epigenetic changes in response to tai chi practice: a pilot investigation of DNA methylation marks
Hua Ren, Veronica Collins, Sandy J Clarke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 27, 2008
A model for offering carrier screening for fragile X syndrome to nonpregnant women: results from a pilot study
Sylvia Metcalfe, Alice Jacques, Alison Archibald, et al.
Orphanet Journal of Rare Diseases
|
November 12, 2022
Clinical management guidelines for Friedreich ataxia: best practice in rare diseases
Louise A Corben, Veronica Collins, Sarah Milne, et al.
Brain : a Journal of Neurology
|
February 2, 2008
Vestibular, saccadic and fixation abnormalities in genetically confirmed Friedreich ataxia
Michael C Fahey, Phillip D Cremer, Swee T Aw, et al.
European Journal of Human Genetics : EJHG
|
January 12, 2012
ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible
Martin B Delatycki, Michelle Wolthuizen, Veronica Collins, et al.
Page
of 3