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Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry
|
May 30, 2006
Effect of calcium tablets on interpretation of lumbar spine DXA scans
David L Kendler, Gary M Kiebzak, Catherine G Ambrose, et al.
Kidney International Reports
|
January 16, 2023
Kidney-Function Trajectories From Young Adulthood to Midlife: Identifying Risk Strata and Opportunities for Intervention
Hayley Guiney, Robert Walker, Jonathan Broadbent, et al.
Revista Da Associacao Medica Brasileira (1992)
|
November 26, 2015
Menkes disease: importance of diagnosis with molecular analysis in the neonatal period
Larissa Sampaio de Athayde Costa, Stephanie Pucci Pegler, Rute Facchini Lellis, et al.
American Journal of Medical Genetics. Part A
|
February 24, 2011
Cantú syndrome: report of nine new cases and expansion of the clinical phenotype
Ingrid Scurr, Louise Wilson, Melissa Lees, et al.
American Journal of Medical Genetics. Part A
|
October 22, 2019
Nosology and classification of genetic skeletal disorders: 2019 revision
Geert R Mortier, Daniel H Cohn, Valerie Cormier-Daire, et al.
European Journal of Medical Genetics
|
October 5, 2010
Lung disease associated with periventricular nodular heterotopia and an FLNA mutation
Alice Masurel-Paulet, Eric Haan, Elizabeth M Thompson, et al.
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry
|
May 9, 2007
Standards and guidelines for technologists performing central dual-energy X-ray absorptiometry
Aliya A Khan, Anita Colquhoun, David A Hanley, et al.
European Journal of Human Genetics : EJHG
|
November 23, 2020
Pathogenic variants causing ABL1 malformation syndrome cluster in a myristoyl-binding pocket and increase tyrosine kinase activity
Alexander J M Blakes, Emily Gaul, Wayne Lam, et al.
American Journal of Medical Genetics. Part A
|
March 26, 2011
Nosology and classification of genetic skeletal disorders: 2010 revision
Matthew L Warman, Valerie Cormier-Daire, Christine Hall, et al.
Neurology
|
August 24, 2012
Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesis
Tiziana Pisano, A James Barkovich, Richard J Leventer, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 39) with videos related to
Sort By:
Page
of 4
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry
|
May 30, 2006
Effect of calcium tablets on interpretation of lumbar spine DXA scans
David L Kendler, Gary M Kiebzak, Catherine G Ambrose, et al.
Kidney International Reports
|
January 16, 2023
Kidney-Function Trajectories From Young Adulthood to Midlife: Identifying Risk Strata and Opportunities for Intervention
Hayley Guiney, Robert Walker, Jonathan Broadbent, et al.
Revista Da Associacao Medica Brasileira (1992)
|
November 26, 2015
Menkes disease: importance of diagnosis with molecular analysis in the neonatal period
Larissa Sampaio de Athayde Costa, Stephanie Pucci Pegler, Rute Facchini Lellis, et al.
American Journal of Medical Genetics. Part A
|
February 24, 2011
Cantú syndrome: report of nine new cases and expansion of the clinical phenotype
Ingrid Scurr, Louise Wilson, Melissa Lees, et al.
American Journal of Medical Genetics. Part A
|
October 22, 2019
Nosology and classification of genetic skeletal disorders: 2019 revision
Geert R Mortier, Daniel H Cohn, Valerie Cormier-Daire, et al.
European Journal of Medical Genetics
|
October 5, 2010
Lung disease associated with periventricular nodular heterotopia and an FLNA mutation
Alice Masurel-Paulet, Eric Haan, Elizabeth M Thompson, et al.
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry
|
May 9, 2007
Standards and guidelines for technologists performing central dual-energy X-ray absorptiometry
Aliya A Khan, Anita Colquhoun, David A Hanley, et al.
European Journal of Human Genetics : EJHG
|
November 23, 2020
Pathogenic variants causing ABL1 malformation syndrome cluster in a myristoyl-binding pocket and increase tyrosine kinase activity
Alexander J M Blakes, Emily Gaul, Wayne Lam, et al.
American Journal of Medical Genetics. Part A
|
March 26, 2011
Nosology and classification of genetic skeletal disorders: 2010 revision
Matthew L Warman, Valerie Cormier-Daire, Christine Hall, et al.
Neurology
|
August 24, 2012
Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesis
Tiziana Pisano, A James Barkovich, Richard J Leventer, et al.
Page
of 4