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The Journal of Surgical Research
|
May 18, 2025
Trauma, Gender, and End-Of-Life Care: A Propensity-Matched Cohort Study Analyzing Disparities in Withdrawal of Life Support
Priya Pathak, Jonathan Laredo, Sonal Swain, et al.
Plos One
|
July 5, 2013
Correction: Enabling Genomic-Phenomic Association Discovery without Sacrificing Anonymity
Raymond D Heatherly, Grigorios Loukides, Joshua C Denny, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
June 24, 2003
Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13
Erika L Nurmi, Michael Dowd, Ovsanna Tadevosyan-Leyfer, et al.
Genetic Epidemiology
|
December 14, 2007
Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasis
Tricia A Thornton-Wells, Jason H Moore, Eden R Martin, et al.
Investigative Ophthalmology & Visual Science
|
May 1, 1997
Exclusion of TIMP3 as a candidate locus in age-related macular degeneration
M A De La Paz, M A Pericak-Vance, F Lennon, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
November 27, 2001
Skin benefits from continuous topical administration of a zinc oxide/petrolatum formulation by a novel disposable diaper
S Baldwin, M R Odio, S L Haines, et al.
American Journal of Human Genetics
|
February 1, 1993
Linkage localization of X-linked Charcot-Marie-Tooth disease
J Bergoffen, J Trofatter, M A Pericak-Vance, et al.
American Journal of Human Genetics
|
March 1, 1992
A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age
R E Tanzi, P C Watkins, G D Stewart, et al.
The Journal of Experimental Medicine
|
April 1, 1985
Hypohaptoglobinemia associated with familial epilepsy
S S Panter, S M Sadrzadeh, P E Hallaway, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 25, 2006
Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?
Shaochun Ma, Thomas L Davis, Marcia A Blair, et al.
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of 100
Search research articles
Search
Showing results (211-220 of 994) with videos related to
Sort By:
Page
of 100
The Journal of Surgical Research
|
May 18, 2025
Trauma, Gender, and End-Of-Life Care: A Propensity-Matched Cohort Study Analyzing Disparities in Withdrawal of Life Support
Priya Pathak, Jonathan Laredo, Sonal Swain, et al.
Plos One
|
July 5, 2013
Correction: Enabling Genomic-Phenomic Association Discovery without Sacrificing Anonymity
Raymond D Heatherly, Grigorios Loukides, Joshua C Denny, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
June 24, 2003
Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13
Erika L Nurmi, Michael Dowd, Ovsanna Tadevosyan-Leyfer, et al.
Genetic Epidemiology
|
December 14, 2007
Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasis
Tricia A Thornton-Wells, Jason H Moore, Eden R Martin, et al.
Investigative Ophthalmology & Visual Science
|
May 1, 1997
Exclusion of TIMP3 as a candidate locus in age-related macular degeneration
M A De La Paz, M A Pericak-Vance, F Lennon, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
November 27, 2001
Skin benefits from continuous topical administration of a zinc oxide/petrolatum formulation by a novel disposable diaper
S Baldwin, M R Odio, S L Haines, et al.
American Journal of Human Genetics
|
February 1, 1993
Linkage localization of X-linked Charcot-Marie-Tooth disease
J Bergoffen, J Trofatter, M A Pericak-Vance, et al.
American Journal of Human Genetics
|
March 1, 1992
A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age
R E Tanzi, P C Watkins, G D Stewart, et al.
The Journal of Experimental Medicine
|
April 1, 1985
Hypohaptoglobinemia associated with familial epilepsy
S S Panter, S M Sadrzadeh, P E Hallaway, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 25, 2006
Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?
Shaochun Ma, Thomas L Davis, Marcia A Blair, et al.
Page
of 100