Research

March 13, 2023 c22central

Research

Many of our members have been very interested in supporting researchers to advance our understanding of Emanuel Syndrome and the

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DISCLAIMER

Chromosome 22 Central is a volunteer based organization. Every effort has been made to ensure the accuracy of the information provided on this website.

Links to other resources are provided solely as a means of further information, and C22C Inc. does not endorse any such resources.

Any information provided to members or the general public is provided for educational purposes only, and is not intended to replace professional advice from doctors or therapists. C22C Inc. representatives, members or board members DO NOT under any circumstances offer medical advice. Our group's purpose is to strictly offer support and basic information. We are run by a group of caring parents and are not trained to offer medical advice. The site contents were developed by Stephanie Rese, Melissa Carter, Murney Rinholm, and Joanna Holmes - Meet the Team. All information we provide is strictly on an information basis only, and should be shared with your own medical professionals.

It is important to understand that when reading facts about specific disorders, that not all people affected will be the same. As with any disorder, there are degrees of severity, and it is important for parents to understand these facts. It is recommended that any information you receive from C22C or it's members be shared with professionals for comments or advice.

Our site does not accept any form of advertising. Any items, books, other websites etc. are posted with the interest of our membership in mind and no monetary benefit is gained from sharing such items.

Any concerns regarding the content of our website can be directed to Stephanie Rese, c22central@gmail.com

Effective date: July 9, 2003

© Chromosome 22 Central, Inc. 2011| Last Modified, July 2023
Chromosome 22 Central Inc. is a Registered US Corporation with 501 (c) (3) Status.

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