Chromosome 22q Deletion

Common Name(s)

Chromosome 22q Deletion

Description for this condition is not yet available.
 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Chromosome 22q Deletion" for support, advocacy or research.

The Dempster Family Foundation

Dedicated to improving the quality of life for those affected by 22q11.2 Deletion Syndrome. We do this through partnerships that positively impact the growing community of 22q families around the world in areas of awareness, research, family support networks, and education.

Last Updated: 5 May 2014

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Chromosome 22q Deletion" for support, advocacy or research.

The Dempster Family Foundation

Dedicated to improving the quality of life for those affected by 22q11.2 Deletion Syndrome. We do this through partnerships that positively impact the growing community of 22q families around the world in areas of awareness, research, family support networks, and education.

http://www.DempsterFoundation.org

Last Updated: 5 May 2014

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General Support Organizations

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General Resources

22Q University Video Library

http://dempsterfamilyfoundation.org/videos/44

Updated 5 May 2014

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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 22q Deletion" returned 2 free, full-text research articles on human participants. First 3 results:

Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndrome.
 

Author(s): P De Mas, N Chassaing, Y Chaix, M-C Vincent, S Julia, G Bourrouillou, P Calvas, E Bieth

Journal: J. Med. Genet.. 2002 Apr;39(4):e17.

 

Last Updated: 31 Dec 1969

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Deletion mapping of chromosome 1p and 22q in pheochromocytoma.
 

Author(s): E Shin, S Fujita, K Takami, H Kurahashi, Y Kurita, T Kobayashi, T Mori, I Nishisho, S Takai

Journal: Jpn. J. Cancer Res.. 1993 Apr;84(4):402-8.

 

To identify the localization of tumor suppressor genes, 22 pheochromocytomas (9 hereditary and 13 sporadic) were examined for loss of heterozygosity (LOH) on the short arm of chromosome 1 and on the long arm of chromosome 22 by using 11 polymorphic DNA markers on each chromosome arm. ...

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 22q Deletion" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

Clinical Trial in 22q13 Deletion Syndrome(Phelan-McDermid Syndrome)
 

Status: Recruiting

Condition Summary: 22q13 Deletion Syndrome; Phelan-McDermid Syndrome

 

Last Updated: 31 Jul 2018

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