Chromosome 3 Duplication Syndrome

Common Name(s)

Chromosome 3 Duplication Syndrome

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Chromosome 3 Duplication Syndrome" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Chromosome 3 Duplication Syndrome" returned 3 free, full-text research articles on human participants. First 3 results:

A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndrome.
 

Author(s): Janel O Johnson, Giovanni Stevanin, Joyce van de Leemput, Dena G Hernandez, Sampath Arepalli, Sylvie Forlani, Reza Zonozi, J Raphael Gibbs, Alexis Brice, Alexandra Durr, Andrew B Singleton

Journal: Mov. Disord.. 2015 Feb;30(2):262-6.

 

The autosomal dominant spinocerebellar ataxias are most commonly caused by nucleotide repeat expansions followed by base-pair changes in functionally important genes. Structural variation has recently been shown to underlie spinocerebellar ataxia types 15 and 20.

Last Updated: 31 Dec 1969

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Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
 

Author(s): Chih-Ping Chen, Yi-Ning Su, Chin-Yuan Hsu, Schu-Rern Chern, Chen-Chi Lee, Yu-Ting Chen, Wen-Lin Chen, Wayseen Wang

Journal: Taiwan J Obstet Gynecol. 2011 Dec;50(4):485-91.

 

To present prenatal molecular cytogenetic diagnosis of mosaicism for terminal 3p deletion and distal 3q duplication using cultured and uncultured amniocytes, and the association with fetoplacental discrepancy.

Last Updated: 31 Dec 1969

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Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).
 

Author(s): P W Allderdice, N Browne, D P Murphy

Journal: Am. J. Hum. Genet.. 1975 Nov;27(6):699-718.

 

Close phenotypic similarity between two cases carrying a rec(3) dup q,inv(3) (p25q21), 12 additional infants from the same inv (3)(p25q21) kindred who lived less than 1 year, and eight cases studied in other medical centers has led us to postulate the existence of a distinct chromosome ...

Last Updated: 31 Dec 1969

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Chromosome 3 Duplication Syndrome" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

Characterization of 3q29 Deletion Syndrome and 3q29 Duplication Syndrome
 

Status: Recruiting

Condition Summary: Microdeletion 3q29 Syndrome; Microduplication 3q29 Syndrome

 

Last Updated: 16 Jan 2018

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