Dr. Wendy Chung explains Simons Searchlight

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To create scientific breakthroughs for rare genetic neurodevelopmental disorders, families and scientists must come together. This is why YOU have to represent yourself in research!

Simons Searchlight is an ambitious research program that is creating an ever-growing database and resource network.

Driven by Science. United by Hope.
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Where we can contact you? We have a kid, 17 year's old. She have syndrome duplication chromosome 16p11.2 in 26genea. She always feel tired, lost balancing, SPD, lost memory on word, to move body, etc. Please help us.
We live in Indonesia.

fransiscacs
visit shbcf.ru