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Molecular Case Studies Manuscript Processing SystemManuscript Processing System for Cold Spring Harbor Molecular Case Studies.
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Manuscript Processing System for Cold Spring Harbor Molecular Case Studies.
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Molecular Case Studies Manuscript Processing System | submit.molecularcasestudies.org Reviews
https://submit.molecularcasestudies.org
Manuscript Processing System for Cold Spring Harbor Molecular Case Studies.
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molecularcasestudies.cshlp.org
Cold Spring Harbor Molecular Case Studies -- Feedback
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Skip to main page content. Thank you for visiting CSH Molecular Case Studies. To help your message go to the correct recipient, please indicate which of the following best describes the subject of your message:. Comments on the content of the site. Subscription problem or question. Website comment or suggestion. None of the above. We regret that we are not staffed to provide responses to inquiries about specific medical conditions or treatments. Would you like a copy of this message sent to yourself?
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Skip to main page content. Head - Advertising Sales and Sponsorship Advertising Account Manager / Classified Advertising Manager. March 2017, 3 (2). Accelerating personalized medicine with functional genomics. Variant in early-onset mitochondrial disease. Fusion in pleomorphic xanthoastrocytoma.
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Table of Contents — March 2017, 3 (2)
http://molecularcasestudies.cshlp.org/content/current
Skip to main page content. March 2017; 3 (2). Integrating functional genomics to accelerate mechanistic personalized medicine. Jeffrey W. Tyner. Cold Spring Harb Mol Case Stud. Mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infant. Sarah U. Morton. Sanjay P. Prabhu. Hart G.W. Lidov. Catherine A. Brownstein. Matthew N. Bainbridge. Alan H. Beggs. Sara O. Vargas. Pankaj B. Agrawal. Cold Spring Harb Mol Case Stud. January 10, 2017. Ronak M. Patel. James T. Lu.
molecularcasestudies.cshlp.org
Progeroid syndrome patients with ZMPSTE24 deficiency could benefit when treated with rapamycin and dimethylsulfoxide
http://molecularcasestudies.cshlp.org/content/3/1/a001339.full
Skip to main page content. Progeroid syndrome patients with ZMPSTE24 deficiency could benefit when treated with rapamycin and dimethylsulfoxide. Anil K. Agarwal. Division of Nutrition and Metabolic Diseases, Center for Human Nutrition, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA;. Molecular and Cellular Imaging, Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA;. And zinc metalloproteinase (.
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Optic atrophy, cataracts, lipodystrophy/lipoatrophy, and peripheral neuropathy caused by a de novo OPA3 mutation
http://molecularcasestudies.cshlp.org/content/3/1/a001156.full
Skip to main page content. Optic atrophy, cataracts, lipodystrophy/lipoatrophy, and peripheral neuropathy caused by a de novo. Stephanie C. Bourne. Katelin N. Townsend. Scott A. Lear. Wyeth W. Wasserman. William T. Gibson. Department of Microbiology and Immunology, Dalhousie University, Halifax, Nova Scotia B3H 4R2, Canada;. Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada;. AIM Medical Imaging, Vancouver, British Columbia V6H 1C9, Canada;. The O...
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Cold Spring Harbor Molecular Case Studies -- Author Information
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Skip to main page content. Cold Spring Harbor Molecular Case Studies. Guidelines for reported data. Open Access publication fees. Data deposition and release. March 2017, 3 (2). Accelerating personalized medicine with functional genomics. Variant in early-onset mitochondrial disease. Fusion in pleomorphic xanthoastrocytoma.
molecularcasestudies.cshlp.org
Cold Spring Harbor Molecular Case Studies -- About the Journal
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Skip to main page content. About Cold Spring Harbor Molecular Case Studies. Read the launch Press Release here. Cold Spring Harbor Molecular Case Studies. Presenting detailed case studies of individuals and small cohorts. Describing more extensive work using larger cohorts and/or functional analyses. Presenting the discovery of a novel variant and/or novel phenotype associated with a known disease gene. Presenting the discovery of a novel variant or combination of variants in a cancer type. DIRECTOR OF P...
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MMCTS Manuscript Processing System
Create a new account. Welcome to the online system. If this is your first time using the system, please create a new account. Remember my email address. Enter the Author Area. Submit a new/revised manuscript. Continue a manuscript submission. Proof a converted manuscript. Check the status of a manuscript. Enter the Reviewer Area. Respond to a review request. Submit or work on a review. Enter the Tracking Area. Perform Section Editor duties. Perform Editorial Staff duties. Update your contact information.
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submit.molecularcasestudies.org
Molecular Case Studies Manuscript Processing System
Create a new account. I have forgotten my password. Welcome to the Molecular Case Studies manuscript processing system. If this is your first time using the system, please create a new account. Remember my email address. Enter the Author Area. Submit a New/Revised Manuscript. Continue a Manuscript Submission. Proof a converted manuscript. Check the Status of a Manuscript. Enter the Reviewer Area. Give comments to the Handling Editor. Or Respond to a Review Request. Submit or Work on Comments or a Review.
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