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American Journal of Medical Genetics. Part A
|
December 25, 2009
CHN1 mutations are not a common cause of sporadic Duane's retraction syndrome
Noriko Miyake, Caroline Andrews, Wen Fan, et al.
Ophthalmology
|
March 12, 2014
Diagnostic distinctions and genetic analysis of patients diagnosed with moebius syndrome
Sarah MacKinnon, Darren T Oystreck, Caroline Andrews, et al.
Journal of Veterinary Pharmacology and Therapeutics
|
October 8, 2021
Anticoagulant profile of subcutaneous enoxaparin in healthy dogs
Julianna Frum, Katie Havill, Caroline Andrews, et al.
Open Mind : Discoveries in Cognitive Science
|
July 7, 2023
The Agent Preference in Visual Event Apprehension
Arrate Isasi-Isasmendi, Caroline Andrews, Monique Flecken, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 7, 2015
Expanding the phenotypic spectrum and variability of endocrine abnormalities associated with TUBB3 E410K syndrome
Ravikumar Balasubramanian, Sheena Chew, Sarah E MacKinnon, et al.
Investigative Ophthalmology & Visual Science
|
July 1, 2011
Expansion of the CHN1 strabismus phenotype
Noriko Miyake, Joseph L Demer, Sherin Shaaban, et al.
JAMA Ophthalmology
|
October 5, 2013
RYR1 mutations as a cause of ophthalmoplegia, facial weakness, and malignant hyperthermia
Sherin Shaaban, Leigh Ramos-Platt, Floyd H Gilles, et al.
Oncotarget
|
June 2, 2018
Inhibiting Janus Kinase 1 and BCL-2 to treat T cell acute lymphoblastic leukemia with IL7-Rα mutations
Emilee Senkevitch, Wenqing Li, Julie A Hixon, et al.
ACS Central Science
|
December 7, 2019
Electrostatically Driven Guanidinium Interaction Domains that Control Hydrogel-Mediated Protein Delivery In Vivo
Stephen E Miller, Yuji Yamada, Nimit Patel, et al.
Ophthalmology
|
May 3, 2011
Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography a predictor of visual acuity?
Mervyn G Thomas, Anil Kumar, Sarim Mohammad, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 83) with videos related to
Sort By:
Page
of 9
American Journal of Medical Genetics. Part A
|
December 25, 2009
CHN1 mutations are not a common cause of sporadic Duane's retraction syndrome
Noriko Miyake, Caroline Andrews, Wen Fan, et al.
Ophthalmology
|
March 12, 2014
Diagnostic distinctions and genetic analysis of patients diagnosed with moebius syndrome
Sarah MacKinnon, Darren T Oystreck, Caroline Andrews, et al.
Journal of Veterinary Pharmacology and Therapeutics
|
October 8, 2021
Anticoagulant profile of subcutaneous enoxaparin in healthy dogs
Julianna Frum, Katie Havill, Caroline Andrews, et al.
Open Mind : Discoveries in Cognitive Science
|
July 7, 2023
The Agent Preference in Visual Event Apprehension
Arrate Isasi-Isasmendi, Caroline Andrews, Monique Flecken, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 7, 2015
Expanding the phenotypic spectrum and variability of endocrine abnormalities associated with TUBB3 E410K syndrome
Ravikumar Balasubramanian, Sheena Chew, Sarah E MacKinnon, et al.
Investigative Ophthalmology & Visual Science
|
July 1, 2011
Expansion of the CHN1 strabismus phenotype
Noriko Miyake, Joseph L Demer, Sherin Shaaban, et al.
JAMA Ophthalmology
|
October 5, 2013
RYR1 mutations as a cause of ophthalmoplegia, facial weakness, and malignant hyperthermia
Sherin Shaaban, Leigh Ramos-Platt, Floyd H Gilles, et al.
Oncotarget
|
June 2, 2018
Inhibiting Janus Kinase 1 and BCL-2 to treat T cell acute lymphoblastic leukemia with IL7-Rα mutations
Emilee Senkevitch, Wenqing Li, Julie A Hixon, et al.
ACS Central Science
|
December 7, 2019
Electrostatically Driven Guanidinium Interaction Domains that Control Hydrogel-Mediated Protein Delivery In Vivo
Stephen E Miller, Yuji Yamada, Nimit Patel, et al.
Ophthalmology
|
May 3, 2011
Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography a predictor of visual acuity?
Mervyn G Thomas, Anil Kumar, Sarim Mohammad, et al.
Page
of 9