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Basic Facts about NUT Midline Carcinoma





Registry Personnel

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It is critical that we continue to collect information on NUT midline carcinoma. We ask all families and physicians who use our information to allow us to collect data on every person with NMC. We ask for your help. Every time we receive an inquiry, we ask to follow the patient.

Families and physicians may initiate the enrollment process. Forms may be downloaded as listed below.

The International NMC Registry is approved on a continuing basis by the institutional review board (IRB) of the Dana-Farber/Harvard Cancer Center.

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