|3p deletion syndrome||0.36||0.9||5346||53|
|shank 3 deletion||1.1||0.6||5966||50|
|system 32 deletion||0.7||0.4||4995||81|
|deletion of 3p14.1||0.99||1||788||31|
|deletion of 3 base pairs||1.84||0.5||3626||33|
|deletion of 3 bases||0.76||0.1||4472||89|
|alpha 3.7 deletion||1.17||0.3||4996||53|
|microsoft 365 deletion policy||1.49||0.3||4940||45|
|chromosome 3p deletion syndrome||0.24||0.9||7783||12|
|3p deletion syndrome genereviews||0.69||0.3||881||24|
|3p deletion syndrome mortality||1.33||1||8040||66|
|3p deletion syndrome symptoms||1.33||0.7||527||58|
3p deletion syndrome is a condition that results from a chromosomal change in which a small piece of chromosome 3 is deleted in each cell. The deletion occurs at the end of the short (p) arm of the chromosome. This chromosomal change often leads to intellectual disability, developmental delay, and abnormal physical features.Where is the deletion of chromosome 3 located?
People with this condition are missing genetic material located on the short arm (p) of chromosome 3 in each cell. The severity of the condition and the associated signs and symptoms vary based on the size and location of the deletion and which genes are involved.Is there a new version of Gard for chromosome 3p partial deletion?
We are currently developing a new version of GARD. This site is in-development and may not reflect the final version. Chromosome 3p partial deletion is a chromosome abnormality that affects many different parts of the body. People with this condition are missing genetic material located on the short arm (p) of chromosome 3 in each cell.What is deletion in medical terms?
Medical Definition of deletion 1 : the absence of a section of genetic material from a gene or chromosome 2 : the mutational process that results in a deletion