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Annals of Neurology
|
June 1, 1996
Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy. The FSH-DY Group
R Tawil, J Forrester, R C Griggs, et al.
Indoor Air
|
March 20, 2013
Association of classroom ventilation with reduced illness absence: a prospective study in California elementary schools
M J Mendell, E A Eliseeva, M M Davies, et al.
Journal of Occupational and Environmental Hygiene
|
April 1, 2006
Indicators of moisture and ventilation system contamination in U.S. office buildings as risk factors for respiratory and mucous membrane symptoms: analyses of the EPA BASE data
Mark J Mendell, Myrna Cozen, Quanhong Lei-Gomez, et al.
Indoor Air
|
August 22, 2014
Effects of ventilation rate per person and per floor area on perceived air quality, sick building syndrome symptoms, and decision-making
R Maddalena, M J Mendell, K Eliseeva, et al.
Environmental Science. Processes & Impacts
|
March 1, 2021
Associations of observed home dampness and mold with the fungal and bacterial dust microbiomes
Jennie Cox, Timothy Stone, Patrick Ryan, et al.
Indoor Air
|
June 3, 2014
Next-generation DNA sequencing reveals that low fungal diversity in house dust is associated with childhood asthma development
K C Dannemiller, M J Mendell, J M Macher, et al.
Indoor Air
|
December 15, 2015
Higher measured moisture in California homes with qualitative evidence of dampness
J M Macher, M J Mendell, K Kumagai, et al.
Indoor Air
|
May 10, 2014
Evaluation of the indoor air quality minimum ventilation rate procedure for use in California retail buildings
S M Dutton, M J Mendell, W R Chan, et al.
American Journal of Human Genetics
|
August 1, 1992
Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35
B Weiffenbach, R Bagley, K Falls, et al.
Clinical Genetics
|
April 13, 2011
Maternal uniparental disomy of chromosome 4 in a patient with limb-girdle muscular dystrophy 2E confirmed by SNP array technology
C E Cottrell, J Mendell, M Hart-Kothari, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 5
Annals of Neurology
|
June 1, 1996
Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy. The FSH-DY Group
R Tawil, J Forrester, R C Griggs, et al.
Indoor Air
|
March 20, 2013
Association of classroom ventilation with reduced illness absence: a prospective study in California elementary schools
M J Mendell, E A Eliseeva, M M Davies, et al.
Journal of Occupational and Environmental Hygiene
|
April 1, 2006
Indicators of moisture and ventilation system contamination in U.S. office buildings as risk factors for respiratory and mucous membrane symptoms: analyses of the EPA BASE data
Mark J Mendell, Myrna Cozen, Quanhong Lei-Gomez, et al.
Indoor Air
|
August 22, 2014
Effects of ventilation rate per person and per floor area on perceived air quality, sick building syndrome symptoms, and decision-making
R Maddalena, M J Mendell, K Eliseeva, et al.
Environmental Science. Processes & Impacts
|
March 1, 2021
Associations of observed home dampness and mold with the fungal and bacterial dust microbiomes
Jennie Cox, Timothy Stone, Patrick Ryan, et al.
Indoor Air
|
June 3, 2014
Next-generation DNA sequencing reveals that low fungal diversity in house dust is associated with childhood asthma development
K C Dannemiller, M J Mendell, J M Macher, et al.
Indoor Air
|
December 15, 2015
Higher measured moisture in California homes with qualitative evidence of dampness
J M Macher, M J Mendell, K Kumagai, et al.
Indoor Air
|
May 10, 2014
Evaluation of the indoor air quality minimum ventilation rate procedure for use in California retail buildings
S M Dutton, M J Mendell, W R Chan, et al.
American Journal of Human Genetics
|
August 1, 1992
Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35
B Weiffenbach, R Bagley, K Falls, et al.
Clinical Genetics
|
April 13, 2011
Maternal uniparental disomy of chromosome 4 in a patient with limb-girdle muscular dystrophy 2E confirmed by SNP array technology
C E Cottrell, J Mendell, M Hart-Kothari, et al.
Page
of 5