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Benjamin D Solomon

Showing results (61-70 of 179) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|June 9, 2020
The Role of Host Genetic Factors in Coronavirus Susceptibility: Review of Animal and Systematic Review of Human LiteratureMarissa LoPresti, David B Beck, Priya Duggal, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Cyclopia (synophthalmia) in Smith-Lemli-Opitz syndrome: First reported case and consideration of mechanismDavid D Weaver, Benjamin D Solomon, Kelly Akin-Samson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 3, 2019
Response to Wang et alMaegan E Roberts, Nur Zeinomar, Benjamin D Solomon, et al.
American Journal of Medical Genetics. Part A|October 6, 2018
Basan gets a new fingerprint: Mutations in the skin-specific isoform of SMARCAD1 cause ectodermal dysplasia syndromes with adermatoglyphiaMonica N Valentin, Benjamin D Solomon, Gabriele Richard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 26, 2018
Response to ten Broeke et alMaegan E Roberts, Nur Zeinomar, Benjamin D Solomon, et al.
Human Genetics|April 7, 2010
Evidence for inheritance in patients with VACTERL associationBenjamin D Solomon, Daniel E Pineda-Alvarez, Manu S Raam, et al.
American Journal of Human Genetics|August 20, 2020
The Role of Host Genetic Factors in Coronavirus Susceptibility: Review of Animal and Systematic Review of Human LiteratureMarissa LoPresti, David B Beck, Priya Duggal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 20, 2018
Response to Evans et alMaegan E Roberts, Nur Zeinomar, Benjamin D Solomon, et al.
Molecular Genetics and Metabolism|April 17, 2012
Molecular analysis of the Noggin (NOG) gene in holoprosencephaly patientsKshitij Srivastava, Ping Hu, Benjamin D Solomon, et al.
American Journal of Medical Genetics. Part A|August 29, 2018
Phenotypic diversity of patients diagnosed with VACTERL associationMajid Husain, Marina Dutra-Clarke, Bryan Lemieux, et al.
Pageof 18

Showing results (61-70 of 179) with videos related to

Sort By:
Pageof 18
Medrxiv : the Preprint Server for Health Sciences|June 9, 2020
The Role of Host Genetic Factors in Coronavirus Susceptibility: Review of Animal and Systematic Review of Human LiteratureMarissa LoPresti, David B Beck, Priya Duggal, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Cyclopia (synophthalmia) in Smith-Lemli-Opitz syndrome: First reported case and consideration of mechanismDavid D Weaver, Benjamin D Solomon, Kelly Akin-Samson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 3, 2019
Response to Wang et alMaegan E Roberts, Nur Zeinomar, Benjamin D Solomon, et al.
American Journal of Medical Genetics. Part A|October 6, 2018
Basan gets a new fingerprint: Mutations in the skin-specific isoform of SMARCAD1 cause ectodermal dysplasia syndromes with adermatoglyphiaMonica N Valentin, Benjamin D Solomon, Gabriele Richard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 26, 2018
Response to ten Broeke et alMaegan E Roberts, Nur Zeinomar, Benjamin D Solomon, et al.
Human Genetics|April 7, 2010
Evidence for inheritance in patients with VACTERL associationBenjamin D Solomon, Daniel E Pineda-Alvarez, Manu S Raam, et al.
American Journal of Human Genetics|August 20, 2020
The Role of Host Genetic Factors in Coronavirus Susceptibility: Review of Animal and Systematic Review of Human LiteratureMarissa LoPresti, David B Beck, Priya Duggal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 20, 2018
Response to Evans et alMaegan E Roberts, Nur Zeinomar, Benjamin D Solomon, et al.
Molecular Genetics and Metabolism|April 17, 2012
Molecular analysis of the Noggin (NOG) gene in holoprosencephaly patientsKshitij Srivastava, Ping Hu, Benjamin D Solomon, et al.
American Journal of Medical Genetics. Part A|August 29, 2018
Phenotypic diversity of patients diagnosed with VACTERL associationMajid Husain, Marina Dutra-Clarke, Bryan Lemieux, et al.
Pageof 18