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It allows people who carry a specific known genetic variant to reduce the likelihood that their children will inherit the condition. Complete My Book Series : My Book My First Book My First Steps to Reading, My a , My B , My C, My D , My E , My F, My G , My H, My I , My J, My K, My L, My M. People with MAP tend to develop multiple adenomatous colon polyps during their lifetime and will have an increased risk of colorectal cancer if they are not monitored closely with regular colonoscopies. However, some polyps can eventually turn malignant, meaning cancerous, and cancers can spread to other parts of the body.

We use the latest encryption technology (SSL) to ensure that your transactions with us are private and protected. Publish or Perish downloads all the references and citations for a given Google Scholar author profile and calculates the h-index among other statistics. The i10-index is a simple measurement that shows how many of the author's papers have 10 or more citations. After selecting a scholar, the program will query Google Scholar for citation data and populate a list of papers, and present summary statistics on the right of this list.

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No missing or damaged pages, no creases or tears, no underlining or highlighting of text, and no writing in the margins. Most recently, in 2008, Jane received the Scholastic Teacher's Choice Award for her outstanding contribution to the My First Steps to Learning Program. When both parents are carriers of a gene change associated with a recessive condition like MAP, there is a 25% chance that a child will inherit 2 altered copies of the gene, causing them to be affected with the disease.This means that the risk of colon polyps and colorectal cancer can be passed from generation to generation in a family. Google Scholar's extensive database might list publications that most academics would not include in an h-index analysis. Recovery of files older than 7 days and younger than 90 days has to be carried out by the ICT Support team. MAP is considered as a possible diagnosis when a person has multiple adenomatous colon polyps but does not have an alteration in the APC gene associated with FAP and AFAP. As we have over 8000 accounts on the system, the amount of space available for each home directory has to be limited.