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Just a few
of the 100+ families who attended C22C's Niagara Picnic, July 22,
2006
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LOOKING
FOR t(11;22) de novo carriers
Dr.
Emanuel's group is trying to examine the mechanism of the
t(11;22) translocation to understand how it happens. They
especially want to find out whether it can happen in female
meiosis as well as in male meiosis. In order to do this, they
look at samples from new translocation carriers, which are rare.
They need to study individuals who have the balanced
translocation, but neither of their parents is a carrier or they
can study individuals who have an Emanuel Syndrome affected
child and neither of them is a carrier. These are what are
called de novo cases. Thus, if there are any de novo carriers
willing to participate in research please email me at steph.stpierre@gmail.com
.
Natural
History of Emanuel Syndrome: A Questionnaire Study
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DONATIONS Please forward a cheque or money order to our US HEAD
OFFICE so that you can obtain a tax receipt.
HEAD OFFICE - for ALL
inquiries: Chromosome 22 Central, c/o Stephanie St-Pierre, 237
Kent Avenue, Timmins, Ontario, Canada P4N 3C2 tel/fax: (705) 268-3099, EMAIL: steph.stpierre@gmail.com
(Stephanie's daughter
is Maia - meet her here)
US Head Office - for US donations: Chromosome 22 Central, c/o
Murney Rinholm, 7108 Partinwood Drive, Fuquay-Varina, North
Carolina, 27526 USA, tel (919) 567-8167, EMAIL: bgr@nc.rr.com
Latin America / Spanish
inquiries - Laura Munoz, Robinson
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© Chromosome 22 Central 2008
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