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S Brooks

Showing results (641-650 of 728) with videos related to

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Physical Review Letters|August 16, 2020
CBETA: First Multipass Superconducting Linear Accelerator with Energy RecoveryA Bartnik, N Banerjee, D Burke, et al.
American Journal of Medical Genetics. Part A|July 23, 2013
Novel no-stop FLNA mutation causes multi-organ involvement in malesRenske Oegema, Jessie M Hulst, Sabine D M Theuns-Valks, et al.
American Journal of Human Genetics|May 11, 2005
Homozygous nonsense mutations in KIAA1279 are associated with malformations of the central and enteric nervous systemsAlice S Brooks, Aida M Bertoli-Avella, Grzegorz M Burzynski, et al.
Annals of Neurology|October 30, 2010
Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron diseaseAgnes A Luty, John B J Kwok, Carol Dobson-Stone, et al.
Open Forum Infectious Diseases|July 17, 2024
High Prevalence of Highly Pathogenic Avian Influenza: A Virus in Vietnam's Live Bird MarketsDuy Tung Dao, Kristen K Coleman, Vuong N Bui, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 21, 2014
No major role for periconceptional folic acid use and its interaction with the MTHFR C677T polymorphism in the etiology of congenital anorectal malformationsCharlotte H W Wijers, Ivo de Blaauw, Nadine Zwink, et al.
Gastroenterology|March 31, 2018
Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung DiseaseYunia Sribudiani, Rajendra K Chauhan, Maria M Alves, et al.
Birth Defects Research|April 17, 2020
Infantile hypertrophic pyloric stenosis in patients with esophageal atresiaChantal A Ten Kate, Rutger W W Brouwer, Yolande van Bever, et al.
Journal of Medical Genetics|October 30, 2007
Hirschsprung disease, associated syndromes and genetics: a reviewJ Amiel, E Sproat-Emison, M Garcia-Barcelo, et al.
Human Molecular Genetics|May 21, 2026
Ultra-rare variants in LAMA2 are risk factors for frontotemporal dementia and motor neuron diseaseHiu Chuen Lok, Carol Dobson-Stone, Marianne Hallupp, et al.
Pageof 73

Showing results (641-650 of 728) with videos related to

Sort By:
Pageof 73
Physical Review Letters|August 16, 2020
CBETA: First Multipass Superconducting Linear Accelerator with Energy RecoveryA Bartnik, N Banerjee, D Burke, et al.
American Journal of Medical Genetics. Part A|July 23, 2013
Novel no-stop FLNA mutation causes multi-organ involvement in malesRenske Oegema, Jessie M Hulst, Sabine D M Theuns-Valks, et al.
American Journal of Human Genetics|May 11, 2005
Homozygous nonsense mutations in KIAA1279 are associated with malformations of the central and enteric nervous systemsAlice S Brooks, Aida M Bertoli-Avella, Grzegorz M Burzynski, et al.
Annals of Neurology|October 30, 2010
Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron diseaseAgnes A Luty, John B J Kwok, Carol Dobson-Stone, et al.
Open Forum Infectious Diseases|July 17, 2024
High Prevalence of Highly Pathogenic Avian Influenza: A Virus in Vietnam's Live Bird MarketsDuy Tung Dao, Kristen K Coleman, Vuong N Bui, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 21, 2014
No major role for periconceptional folic acid use and its interaction with the MTHFR C677T polymorphism in the etiology of congenital anorectal malformationsCharlotte H W Wijers, Ivo de Blaauw, Nadine Zwink, et al.
Gastroenterology|March 31, 2018
Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung DiseaseYunia Sribudiani, Rajendra K Chauhan, Maria M Alves, et al.
Birth Defects Research|April 17, 2020
Infantile hypertrophic pyloric stenosis in patients with esophageal atresiaChantal A Ten Kate, Rutger W W Brouwer, Yolande van Bever, et al.
Journal of Medical Genetics|October 30, 2007
Hirschsprung disease, associated syndromes and genetics: a reviewJ Amiel, E Sproat-Emison, M Garcia-Barcelo, et al.
Human Molecular Genetics|May 21, 2026
Ultra-rare variants in LAMA2 are risk factors for frontotemporal dementia and motor neuron diseaseHiu Chuen Lok, Carol Dobson-Stone, Marianne Hallupp, et al.
Pageof 73