What does S mean in HUMAN GENOME
What does the S mean in HUMAN GENOME? This page is about the meanings of the acronym/abbreviation S in the MEDICAL field. S is most commonly used in the HUMAN GENOME terminology.
S meaning in Human Genome in Medical
S mostly used in an acronym Human Genome in Category Medical that means A Rare Genetic Disorder Characterized By An Uncoordinated Or Clumsy Manner Of Walking Abnormal Gait And Dystonia
Shorthand: S,
Full Form: A Rare Genetic Disorder Characterized By An Uncoordinated Or Clumsy Manner Of Walking Abnormal Gait And Dystonia
For more information of "A Rare Genetic Disorder Characterized By An Uncoordinated Or Clumsy Manner Of Walking Abnormal Gait And Dystonia", see the section below.
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What Questions Are Stands For S? |
There is no one answer to this question as "MISCELLANEOUS, INTERNATIONAL, SCIENCE, MEDICAL" all categories for anything that doesn't fit into another category. It can stand for anything from "leftover" items to items that are difficult to classify. |
Acronyms finder: Look at S related acronym, abbreviation or shorthand.
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