Chromosome 11

Common Name(s)

Chromosome 11

Description for this condition is not yet available.
 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Chromosome 11" for support, advocacy or research.

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11q Research and Resource Group

To provide support and organizational efforts for parents of all children with 11th chromosome abnormalities. Through networking, cooperation with the research community, and resulting sharing of information, we will be better able to meet the challenges brought to us as parents, families and friends of 11q children.

Last Updated: 1 Feb 2013

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General Support Organizations

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How do you compare to others with this condition?

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Chromosome 11" for support, advocacy or research.

Logo
11q Research and Resource Group

To provide support and organizational efforts for parents of all children with 11th chromosome abnormalities. Through networking, cooperation with the research community, and resulting sharing of information, we will be better able to meet the challenges brought to us as parents, families and friends of 11q children.

http://www.11qusa.org/index.htm

Last Updated: 1 Feb 2013

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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 11" returned 256 free, full-text research articles on human participants. First 3 results:

Spectrum of genes involved in a unique case of Potocki Schaffer syndrome with a large chromosome 11 deletion.
 

Author(s): Bernd F M Romeike, Yiping Shen, Hiromi Koso Nishimoto, Cynthia C Morton, Lawrence C Layman, Hyung-Goo Kim

Journal: Clin. Neuropathol.. ;33(3):238-44.

 

Last Updated: 30 Apr 2014

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ENU mutation mapped to a distal region of chromosome 11 is a major determinant of bone size.
 

Author(s): Bouchra Edderkaoui, Chandrasekhar Kesavan, David J Baylink, Jon E Wergedal, Apurva K Srivastava, Subburaman Mohan

Journal: Physiol. Genomics. 2013 Dec;45(24):1222-8.

 

Using a phenotype driven n-ethyl-nitrosourea (ENU) screen in growth hormone-deficient mice, we have identified a mutant (named 14104) that exhibited a smaller bone size. Phenotype measurements by microcomputed tomography revealed that mutant mice exhibited a 43 and 34% reduction in ...

Last Updated: 17 Dec 2013

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Complex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2.
 

Author(s): Thorsten Klampfl, Jelena D Milosevic, Ana Puda, Andreas Schönegger, Klaudia Bagienski, Tiina Berg, Ashot S Harutyunyan, Bettina Gisslinger, Elisa Rumi, Luca Malcovati, Daniela Pietra, Chiara Elena, Matteo Giovanni Della Porta, Lisa Pieri, Paola Guglielmelli, Christoph Bock, Michael Doubek, Dana Dvorakova, Nada Suvajdzic, Dragica Tomin, Natasa Tosic, Zdenek Racil, Michael Steurer, Sonja Pavlovic, Alessandro M Vannucchi, Mario Cazzola, Heinz Gisslinger, Robert Kralovics

Journal:

 

Exome sequencing of primary tumors identifies complex somatic mutation patterns. Assignment of relevance of individual somatic mutations is difficult and poses the next challenge for interpretation of next generation sequencing data. Here we present an approach how exome sequencing ...

Last Updated: 22 Oct 2013

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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 11" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

There are currently no related results available in GeneReviews.

There are currently no related results available in Genetic Testing Registry.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

Genetics and Psychopathology in the 22q11 Deletion Syndrome
 

Status: Recruiting

Condition Summary: Chromosome 22q11.2 Deletion Syndrome

 

Last Updated: 12 Oct 2006

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Last Updated: 21 Feb 2014

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Immunologic Evaluation in Patients With DiGeorge Syndrome or Velocardiofacial Syndrome
 

Status: Recruiting

Condition Summary: DiGeorge Syndrome; Shprintzen Syndrome; Chromosome Abnormalities; Abnormalities, Multiple; Conotruncal Cardiac Defects

 

Last Updated: 23 Jun 2005

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