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Showing results (51-60 of 63) with videos related to

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Msystems|April 5, 2019
Genome and Functional Characterization of Colonization Factor Antigen I- and CS6-Encoding Heat-Stable Enterotoxin-Only Enterotoxigenic <i>Escherichia coli</i> Reveals Lineage and Geographic VariationTracy H Hazen, Sushma Nagaraj, Sunil Sen, et al.
Journal of Bacteriology|April 1, 2014
Streptococcus mutans NADH oxidase lies at the intersection of overlapping regulons controlled by oxygen and NAD+ levelsJ L Baker, A M Derr, K Karuppaiah, et al.
American Journal of Human Genetics|December 1, 1996
Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locusE V Semina, N A Datson, N J Leysens, et al.
Human Genetics|February 24, 2001
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North AmericaM T Bassi, A A Bergen, P Bitoun, et al.
Nature Genetics|December 1, 1996
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndromeE V Semina, R Reiter, N J Leysens, et al.
Journal of Medical Genetics|May 1, 2007
Genotype phenotype correlation of 30 patients with Smith-Magenis syndrome (SMS) using comparative genome hybridisation array: cleft palate in SMS is associated with larger deletionsJ Andrieux, C Villenet, S Quief, et al.
Clinical Genetics|February 24, 2017
Chondrodysplasia with multiple dislocations: comprehensive study of a series of 30 casesE Ranza, C Huber, N Levin, et al.
American Journal of Human Genetics|September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.
Human Genetics|February 24, 2010
Identification of 28 novel mutations in the Bardet-Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous diseaseJean Muller, C Stoetzel, M C Vincent, et al.
American Journal of Human Genetics|June 21, 2002
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafnessL M Astuto, J M Bork, M D Weston, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Msystems|April 5, 2019
Genome and Functional Characterization of Colonization Factor Antigen I- and CS6-Encoding Heat-Stable Enterotoxin-Only Enterotoxigenic <i>Escherichia coli</i> Reveals Lineage and Geographic VariationTracy H Hazen, Sushma Nagaraj, Sunil Sen, et al.
Journal of Bacteriology|April 1, 2014
Streptococcus mutans NADH oxidase lies at the intersection of overlapping regulons controlled by oxygen and NAD+ levelsJ L Baker, A M Derr, K Karuppaiah, et al.
American Journal of Human Genetics|December 1, 1996
Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locusE V Semina, N A Datson, N J Leysens, et al.
Human Genetics|February 24, 2001
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North AmericaM T Bassi, A A Bergen, P Bitoun, et al.
Nature Genetics|December 1, 1996
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndromeE V Semina, R Reiter, N J Leysens, et al.
Journal of Medical Genetics|May 1, 2007
Genotype phenotype correlation of 30 patients with Smith-Magenis syndrome (SMS) using comparative genome hybridisation array: cleft palate in SMS is associated with larger deletionsJ Andrieux, C Villenet, S Quief, et al.
Clinical Genetics|February 24, 2017
Chondrodysplasia with multiple dislocations: comprehensive study of a series of 30 casesE Ranza, C Huber, N Levin, et al.
American Journal of Human Genetics|September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.
Human Genetics|February 24, 2010
Identification of 28 novel mutations in the Bardet-Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous diseaseJean Muller, C Stoetzel, M C Vincent, et al.
American Journal of Human Genetics|June 21, 2002
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafnessL M Astuto, J M Bork, M D Weston, et al.
Pageof 7