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Jacobsen Syndrome

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Jacobsen Syndrome (11q Deletion, or 11q-) is a rare chromosomal abnormality which affects perhaps one child in 100,000 in which a portion of the 11th chromosome is missing. It was discovered by Dr. P. Jacobsen in 1973. At that time, the disease was named "Jacobsen Syndrome."

1. The Fragile WEB Site - Includes a reference database, family support groups and clinical information.



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