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K Zalewski

Showing results (51-60 of 58) with videos related to

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Journal of Neuroscience Methods|September 24, 2018
All-night functional magnetic resonance imaging sleep studiesThomas M Moehlman, Jacco A de Zwart, Miranda G Chappel-Farley, et al.
Human Mutation|February 11, 2009
Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?Byung Yoon Choi, Andrew K Stewart, Anne C Madeo, et al.
Journal of Medical Genetics|September 24, 2011
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotesJulie M Schultz, Rashid Bhatti, Anne C Madeo, et al.
Journal of Medical Genetics|April 21, 2016
Cystic cerebellar dysplasia and biallelic LAMA1 mutations: a lamininopathy associated with tics, obsessive compulsive traits and myopia due to cell adhesion and migration defectsThierry Vilboux, May Christine V Malicdan, Yun Min Chang, et al.
JAMA|March 18, 2024
Clinical, Biomarker, and Research Tests Among US Government Personnel and Their Family Members Involved in Anomalous Health IncidentsLeighton Chan, Mark Hallett, Chris K Zalewski, et al.
JAMA|March 18, 2024
Neuroimaging Findings in US Government Personnel and Their Family Members Involved in Anomalous Health IncidentsCarlo Pierpaoli, Amritha Nayak, Rakibul Hafiz, et al.
Genetics in Medicine Open|July 15, 2025
Systematic phenotype and genotype characterization of Moebius syndromeBryn D Webb, Julie A Jurgens, Narisu Narisu, et al.
Physical Review Letters|October 6, 2000
Charged-particle multiplicity near midrapidity in central Au+Au collisions at sqrt[SNN]=56 and 130 GeVB B Back, M D Baker, D S Barton, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Journal of Neuroscience Methods|September 24, 2018
All-night functional magnetic resonance imaging sleep studiesThomas M Moehlman, Jacco A de Zwart, Miranda G Chappel-Farley, et al.
Human Mutation|February 11, 2009
Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?Byung Yoon Choi, Andrew K Stewart, Anne C Madeo, et al.
Journal of Medical Genetics|September 24, 2011
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotesJulie M Schultz, Rashid Bhatti, Anne C Madeo, et al.
Journal of Medical Genetics|April 21, 2016
Cystic cerebellar dysplasia and biallelic LAMA1 mutations: a lamininopathy associated with tics, obsessive compulsive traits and myopia due to cell adhesion and migration defectsThierry Vilboux, May Christine V Malicdan, Yun Min Chang, et al.
JAMA|March 18, 2024
Clinical, Biomarker, and Research Tests Among US Government Personnel and Their Family Members Involved in Anomalous Health IncidentsLeighton Chan, Mark Hallett, Chris K Zalewski, et al.
JAMA|March 18, 2024
Neuroimaging Findings in US Government Personnel and Their Family Members Involved in Anomalous Health IncidentsCarlo Pierpaoli, Amritha Nayak, Rakibul Hafiz, et al.
Genetics in Medicine Open|July 15, 2025
Systematic phenotype and genotype characterization of Moebius syndromeBryn D Webb, Julie A Jurgens, Narisu Narisu, et al.
Physical Review Letters|October 6, 2000
Charged-particle multiplicity near midrapidity in central Au+Au collisions at sqrt[SNN]=56 and 130 GeVB B Back, M D Baker, D S Barton, et al.
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