Web{"jsonapi":{"version":"1.0","meta":{"links":{"self":{"href":"http:\/\/jsonapi.org\/format\/1.0\/"}}}},"data":{"type":"node--article","id":"7a065dee-37c8-4be5-9656 ... WebThe chromosome 9q subtelomeric deletion represents one of the most common subtelomeric deletions (6%). The syndrome can be caused either by a 9q34.3 microdeletion or by mutations in the EHMT1 gene, which is involved in histone methylation. Affected individuals invariably have severe hypotonia, with speech and gross motor delay.
Novel deletion variants of 9q13–q21.12 and classical euchromatic …
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