Simons Searchlight | 幸运5官网：2025幸运澳洲5官方历史记录查询-澳洲5的官网最新幸运五结果号码 Driven by science. United by hope.

168澳洲幸运5历史开奖记录查询 168网澳洲幸运5开奖结果 Driven by science. United by hope.

To create scientific breakthroughs for rare genetic neurodevelopmental disorders, families and scientists must work together. Simons Searchlight is building an ever growing natural history database, biorepository, and resource network. Families like yours are key to meaningful progress.

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168幸运澳洲5历史开奖记录 About Us

Simons Searchlight studies genes that cause rare neurodevelopmental disorders. The study is international, and families can participate in several languages. Learn More

8047

REGISTERED

Participants with genetic variants registered

7435

CONSENTED

Participants consented to participate

5838

APPROVED

Genetic lab reports approved

80829

SURVEYED

Participant surveys completed

幸运五分钟快速查询澳洲结果-历史结果 Genetic Disorders We Study

We study over 185 genes that cause rare neurodevelopmental disorders, and our list is always expanding. Join us if you or your family member have been diagnosed with one of these genetic conditions.

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澳洲幸运5开奖官网结果查询官方-幸运澳洲5开奖历史记录 How to Join Our Research

Please follow the steps below.

step 1

step 2

Provide your genetic lab report

step 3

Share your medical history

step 4

Fill out surveys

step 5

Provide a blood sample if you are interested

step 6

Update us every year and continue your participation

join us today

168澳洲5历史开奖记录官方 News and Updates

幸运五分钟快速查询澳洲结果 Family Story

The Pettus' Journey with HECW2

Discover the inspiring story of the Pettuses.

Family Story

The Erros' Journey with SCN2A

Discover the inspiring story of the Erros.

Announcement

New ORCA Survey: Measuring Communication in Rare Neurodevelopmental Disorders

ORCA offers a more comprehensive and accurate understanding of communication abilities.

View All

澳洲幸运5开奖结果历史查询与更新 Stay connected with Simons Searchlight

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站长工具 - 澳洲幸运5五分钟幸运澳洲彩开奖结果直播 Participant Voices

Simons Searchlight seems like an amazing way to create a large community and bring more research and awareness to many small communities that might not otherwise have such a big voice.

Stacey, Parent

Every time I complete a survey, I know I am doing my part in advancing research to help my child.

Andrew, Parent

There's been an unexpected amount of peace from sharing our struggles and victories with others.

Katie, Parent

I'd do anything to help my son have the best possible chance for a long and happy life including contributing his medical history and completing surveys in Simons Searchlight!

Vanessa, Parent

Every step we take, every test we do, every survey we fill out....all leads to more information. This data can be studied and processed into real life-changing information.

Rhiannon, Parent

The first myth about caring for someone with special needs is that you are alone. You are not.

Tony, Parent

澳洲168幸运5开奖结果 168澳洲幸运5查询 Explore

Community

Connect with others on private Facebook groups. Find your genetic community’s webpage and select “Support Resources”.

Expertise

Visit our video library to hear insights from our geneticists, scientists, and staff.

Knowledge

Explore dedicated pages for each genetic condition that we study.

Ready to share your unique insights?
You could hold the clues scientists need to make progress and find answers.

join us today