Chromosome 15 (human) - Wikipedia

... Chromosome 15 is one of the 23 pairs of chromosomes in humans. ... Chromosome 15 likely contains between 700 and 900 genes. ... This chromosomal change deletes the region of chromosome...
http://en.wikipedia.org/wiki/Chromosome_15_(human)

 

Chromosome Disorders - Patient UK

Chromosome Disorders / UK sources of information and / or support / See our genetic disease and syndromes page / Disclaimer: Patient UK has no control of the content of the above links. Inclusion does not imply endorsement by Patient UK. Want to...
http://www.patient.co.uk/showdoc/785/

 

Isodicentric 15 : Background - Contact a Family Directory

skip banner - Return to original view / site viewing options / home| about us| publications| / news| shop| translations| ... The extra piece of chromosome 15 has been duplicated end-to-end like a mirror image and is referred...
http://www.cafamily.org.uk/Direct/i17.html

 

BioMed Central |Abstract |Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15

Log on / register / Feedback | / Support / BMC Genetics / Volume 9 ... The duplications most often take the form of a supernumerary pseudodicentric derivative chromosome 15 [der(15)] that has been called inverted duplication...
http://www.biomedcentral.com/1471-2156/9/2/abstract

 

24Dr.com Reference Library Congenital conditions - Genetics of Prader-Willi Syndrome

Search for in / All of 24Dr.com / Contact points / Dictionary / Encyclopaedia / eShop / Library ... A small deletion on chromosome 15. Chromosome 15 maternal disomy. A translocation of chromosomes...
http://www.24dr.com/reference/library/congenital/prader_willi/genetics.htm

 

Prader-Willi Syndrome

Medic8® Genetic Disorders ... Prader-Willi syndrome is a chromosomal condition related to chromosome 15. ... This condition is caused by the loss of active genes in a specific region of chromosome 15.
http://www.medic8.com/genetics/prader-willi-syndrome.htm

 

Trisomy, Monosomy, Ring Chromosome 20p and Genetic Imprinting

Mad Cow Home ... Best Links ... Search this site / Chromosomal abnormalities involving the prion gene / Experimental recommendations / References / Trisomy in chromosome 20p ... Among the first 100 cases enrolled in the project, abnormalities of...
http://www.mad-cow.org/chr20_rings_trisomy.html

 

BBC - Health - Conditions - Angelman syndrome

Home / TV / Radio / Talk / Where I Live / A-Z Index / 7 May 2008 / Accessibility help / Text only / BBC Homepage / Lifestyle / Health ... Chromosome 15 is almost unique in that it carries an imprinted region, which means that...
http://www.bbc.co.uk/health/conditions/angelman1.shtml

 

e-Prints Soton - FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation

FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation ... Fluorescence in situ hybridisation studies using chromosome 15-specific probes characterised the presence of seven...
http://eprints.soton.ac.uk/24656/

 

Prader-Willi Syndrome

Disorder Information Sheet ... Prader-Willi Syndrome (PWS) is an inherited disorder genetic disorder which is generally caused by a deletion in Chromosome 15. ... A small deletion on chromosome 15.
http://www.psychnet-uk.com/dsm_iv/prader_willi.htm

 
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