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Showing results (241-250 of 246) with videos related to

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Transactions of the Royal Society of Tropical Medicine and Hygiene|January 1, 1977
Arbovirus isolations from mosquitoes: Kano Plain, KenyaB K Johnson, P Shockley, A C Chanas, et al.
Journal of Epidemiology and Community Health|April 16, 2005
Trends in smoking behaviour between 1985 and 2000 in nine European countries by educationK Giskes, A E Kunst, J Benach, et al.
Pediatrics|March 2, 1999
Silent cerebral infarcts in sickle cell anemia: a risk factor analysis. The Cooperative Study of Sickle Cell DiseaseT R Kinney, L A Sleeper, W C Wang, et al.
Physiological Genomics|June 11, 2009
Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing lossPu Dai, Andrew K Stewart, Fouad Chebib, et al.
The New England Journal of Medicine|January 11, 2008
Association between microdeletion and microduplication at 16p11.2 and autismLauren A Weiss, Yiping Shen, Joshua M Korn, et al.
Nature|September 2, 2011
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locusSébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.
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Showing results (241-250 of 246) with videos related to

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Pageof 25
You have reached the last page of results.This site can display upto 246 results.
Transactions of the Royal Society of Tropical Medicine and Hygiene|January 1, 1977
Arbovirus isolations from mosquitoes: Kano Plain, KenyaB K Johnson, P Shockley, A C Chanas, et al.
Journal of Epidemiology and Community Health|April 16, 2005
Trends in smoking behaviour between 1985 and 2000 in nine European countries by educationK Giskes, A E Kunst, J Benach, et al.
Pediatrics|March 2, 1999
Silent cerebral infarcts in sickle cell anemia: a risk factor analysis. The Cooperative Study of Sickle Cell DiseaseT R Kinney, L A Sleeper, W C Wang, et al.
Physiological Genomics|June 11, 2009
Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing lossPu Dai, Andrew K Stewart, Fouad Chebib, et al.
The New England Journal of Medicine|January 11, 2008
Association between microdeletion and microduplication at 16p11.2 and autismLauren A Weiss, Yiping Shen, Joshua M Korn, et al.
Nature|September 2, 2011
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locusSébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.
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