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American Journal of Medical Genetics. Part A
|
March 5, 2021
Partners in care
Margaret G Au
Molecular and Cellular Endocrinology
|
June 14, 2011
Genetic counseling for isolated GnRH deficiency
Margaret G Au, William F Crowley, Cassandra L Buck
Journal of Genetic Counseling
|
October 9, 2009
Decisions to seek healthcare based on family health history among urban Appalachian women
Robyn A Cree, John Lynch, Margaret G Au, et al.
Journal of Genetic Counseling
|
October 24, 2020
Evaluating co-created patient-facing materials to increase understanding of genetic test results
Andrew A Dwyer, Margaret G Au, Neil Smith, et al.
Annals of Clinical and Translational Neurology
|
September 26, 2018
<i>FARS2</i> mutations presenting with pure spastic paraplegia and lesions of the dentate nuclei
Supreet K Sahai, Rebecca E Steiner, Margaret G Au, et al.
Preventing Chronic Disease
|
December 31, 2009
Familial risk for chronic disease and intent to share family history with a health care provider among urban Appalachian women, southwestern Ohio, 2007
Margaret G Au, Sandra J Cornett, Todd G Nick, et al.
Clinical Genetics
|
May 27, 2025
ACTC1 Variants Result in Isolated and Syndromic Cardiac Phenotypes
Yuri A Zarate, Lina Abdelmoti, Seungjae Oh, et al.
Endocrine Reviews
|
November 2, 2010
The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutations
Cecilia Martin, Ravikumar Balasubramanian, Andrew A Dwyer, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 11, 2011
Olfactory phenotypic spectrum in idiopathic hypogonadotropic hypogonadism: pathophysiological and genetic implications
Hilana M Lewkowitz-Shpuntoff, Virginia A Hughes, Lacey Plummer, et al.
Progress in Community Health Partnerships : Research, Education, and Action
|
March 9, 2010
A family history demonstration project among women in an urban Appalachian community
Jody P Wallace, Carol Baugh, Sandra Cornett, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
American Journal of Medical Genetics. Part A
|
March 5, 2021
Partners in care
Margaret G Au
Molecular and Cellular Endocrinology
|
June 14, 2011
Genetic counseling for isolated GnRH deficiency
Margaret G Au, William F Crowley, Cassandra L Buck
Journal of Genetic Counseling
|
October 9, 2009
Decisions to seek healthcare based on family health history among urban Appalachian women
Robyn A Cree, John Lynch, Margaret G Au, et al.
Journal of Genetic Counseling
|
October 24, 2020
Evaluating co-created patient-facing materials to increase understanding of genetic test results
Andrew A Dwyer, Margaret G Au, Neil Smith, et al.
Annals of Clinical and Translational Neurology
|
September 26, 2018
<i>FARS2</i> mutations presenting with pure spastic paraplegia and lesions of the dentate nuclei
Supreet K Sahai, Rebecca E Steiner, Margaret G Au, et al.
Preventing Chronic Disease
|
December 31, 2009
Familial risk for chronic disease and intent to share family history with a health care provider among urban Appalachian women, southwestern Ohio, 2007
Margaret G Au, Sandra J Cornett, Todd G Nick, et al.
Clinical Genetics
|
May 27, 2025
ACTC1 Variants Result in Isolated and Syndromic Cardiac Phenotypes
Yuri A Zarate, Lina Abdelmoti, Seungjae Oh, et al.
Endocrine Reviews
|
November 2, 2010
The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutations
Cecilia Martin, Ravikumar Balasubramanian, Andrew A Dwyer, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 11, 2011
Olfactory phenotypic spectrum in idiopathic hypogonadotropic hypogonadism: pathophysiological and genetic implications
Hilana M Lewkowitz-Shpuntoff, Virginia A Hughes, Lacey Plummer, et al.
Progress in Community Health Partnerships : Research, Education, and Action
|
March 9, 2010
A family history demonstration project among women in an urban Appalachian community
Jody P Wallace, Carol Baugh, Sandra Cornett, et al.
Page
of 2