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CSOA Forte Prenestino is a large self-managed social centre based in a squatted fort in Centocelle, Rome. It was occupied on May Day 1986. Forte Prenestino ...
Missing: U %22q% 3D% 22
attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but ...
Missing: sa= U %22q% 3D% 22
DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by a microdeletion on the long arm of chromosome 22. While the symptoms can ...
Missing: 3D% CSOA Forte Prenestino
22q11.2 distal deletion syndrome is a rare genetic condition caused by a tiny missing part of one of the body's 46 chromosomes – chromosome 22.
Missing: U 3D% CSOA Forte Prenestino
22q13 deletion syndrome, known as Phelan–McDermid syndrome (PMS), is a genetic disorder caused by deletions or rearrangements on the q terminal end (long ...
Missing: U 3D% CSOA Forte Prenestino
22q11.2 deletion syndrome is a genetic condition that affects many parts of the body. It can cause intellectual disability, learning and social challenges, and ...
Missing: sa= 3D% m. wikipedia. wiki/ CSOA Forte Prenestino
Individuals with 22q11.2 deletion syndrome (22q11.2DS) can present with a wide range of features that are highly variable, even within families.
Missing: 3D% wikipedia. wiki/ CSOA Forte Prenestino
2 Deletion syndrome or 22q (also referred to as Velocardiofacialsyndrome (VCFS), and/or DiGeorge syndrome) is a disorder caused by a small missing piece of the ...
Missing: sa= 3D% wikipedia. wiki/ CSOA Forte Prenestino
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