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Check out the latest news. From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. For more information about the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. The Consortium provides the largest available sample to date. 1000 genetically and phenotypically characterized individuals with 22q11DS. The latest genomic data is available here. The latest phenotypic data is available here.

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Check out the latest news. From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. For more information about the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. The Consortium provides the largest available sample to date. 1000 genetically and phenotypically characterized individuals with 22q11DS. The latest genomic data is available here. The latest phenotypic data is available here.

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22q11-ibbc.org | HOME | dstanalytics.com Reviews

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Check out the latest news. From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. For more information about the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. The Consortium provides the largest available sample to date. 1000 genetically and phenotypically characterized individuals with 22q11DS. The latest genomic data is available here. The latest phenotypic data is available here.

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22q11-ibbc.org | Member Sites

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Member Sites and Participants. Emory University - PI: Stephen Warren, Ph.D. (Lead Site). Albert Einstein College of Medicine - PI: Bernice Morrow Ph.D. CHOP - PI: Beverly Emanuel, Ph.D. Leuven - PI: Joris Vermeesch, Ph.D. Toronto - PI: Steve Sherer, Ph.D. Canada, Australia, and Chile (CAN ). Toronto, Canada - PIs: Anne Bassett, M.D. and Eva Chow, M.D. (Lead Site). Newcastle, Australia - PI: Linda Campbell, Ph.D. Santiago, Chile - PI: Gabriela Repetto, M.D. Geneva, Switzerland - PI: Stephen Eliez, M.D.

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22q11-ibbc.org | Publications

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Publications by Consortium Members. Variant discovery and breakpoint region prediction for studying the human 22q11.2 deletion using BAC clone and whole genome sequencing analysis. Guo X, Delio M, Haque N, Castellanos R, Hestand MS, Vermeesch JR, Morrow BE, Zheng D. Hum Mol Genet. (In press) doi:10.1093/hmg/ddw221. Download PDF. The use of two different MLPA kits in 22q11.2 deletion syndrome. Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome. Overt cleft palate pheno...

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22q11-ibbc.org | Login

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2015 - 2016 Department of Genetics, Albert Einstein College of Medicine, Bronx NY USA.

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22q11-ibbc.org | Announcements

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March 7, 2016. Added 100 new subjects. February 19, 2016. Added 129 new subjects and updated the publication list. January 6, 2016. Added 116 new subjects to genomic database. NOVEMBER 23, 2015. Added 229 new subjects to genomic database. NOVEMBER 06, 2015. Added 26 new subjects to genomic database. OCTOBER 27, 2015. Added 347 new subjects to genomic database. SEPTEMBER 10, 2015. Added 229 new subjects to genomic database. AUGUST 10, 2015. Added 127 new subjects to genomic database. JUNE 22, 2015.

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22q11-ibbc.org | HOME

Check out the latest news. From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. For more information about the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. The Consortium provides the largest available sample to date. 1000 genetically and phenotypically characterized individuals with 22q11DS. The latest genomic data is available here. The latest phenotypic data is available here.

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