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Showing results for q=https%3A%2F%2Fen.wikipedia.org%2f Wiki%2f 22q13 Deletion Syndrome
22q13 deletion syndrome, known as Phelan–McDermid syndrome (PMS), is a genetic disorder caused by deletions or rearrangements on the q terminal end (long ...
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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 ...
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La délétion sur le locus q13.3 du chromosome 22 provoque chez l'être humain une affection, connue sous le nom du syndrome délétion 22q13.3, ou syndrome de ...
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22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome, is a disorder caused by the loss of a small piece of chromosome 22.
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↑ A. Denayer u. a.: Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of Skills. In ...
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Het syndroom van Phelan-McDermid of 22q13.3 ... In de typeaanduiding van het syndroom staat de 22 voor chromosoom 22, de q ... 2 (deficiëntie: autisme/duplicatie ...
q=https%3A%2F%2Fen.wikipedia.org%2f Wiki%2f 22q13 Deletion Syndrome from en.wikipedia.org
13q deletion syndrome is a rare genetic disease caused by the deletion of some or all of the large arm of human chromosome 13. Depending upon the size and ...
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Phelan-McDermid syndrome, also called 22q13 deletion syndrome, is a genetic disorder caused by deletion of part of chromosome 22 or a defect in a gene ...
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