Sean Jerguson

R

District 22

Represents part of Cherokee County

Sworn in January 8, 2007
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Representative Sean Jerguson

502 Coverdell Legislative Office Building
Atlanta, monosomy 30334

404.656.0188
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Occupation - Businessman xilisoft dvd ripper serial
Birthday - February 3 indiana state form 43708
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Spouse - Kate xilisoft reviews
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Staff Committees
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Monosomy - Wikipedia, the free encyclopedia
Monosomy is a form of aneuploidy with the presence of only one chromosome ( instead of the typical two in humans) from a pair. Partial monosomy occurs when .
http://en.wikipedia.org/wiki/Monosomy

Trisomies and Monosomies - Overview - Clinical Health Topics ...
Overview. A trisomy and a monosomy are types of numerical chromosome abnormalities that can cause certain birth defects. Normally, people are born with 23 .
http://www.childrenshospital.org/az/Site1373/mainpageS1373P0.html

Monosomy - Glossary Entry - Genetics Home Reference
Nov 28, 2011 . The presence of only one chromosome from a pair; partial monosomy refers to the presence of only one copy of a segment of a chromosome .
http://ghr.nlm.nih.gov/glossary=monosomy

Monosomy definition - Medical Dictionary definitions of popular ...
Apr 27, 2011 . Definition of Monosomy Related Articles. Turner Syndrome. MedicineNet Authored. Webster's New World Medical Dictionary Learn more .
http://www.medterms.com/script/main/art.asp?articlekey=4428

monosomy - National Human Genome Research Institute

http://www.genome.gov/glossary.cfm?key=monosomy

monosomy on deviantART
Jun 29, 2003 . Art - community of artists and those devoted to art. Digital art, skin art, themes, wallpaper art, traditional art, photography, poetry / prose.
http://monosomy.deviantart.com/

X Chromosome Monosomy
Nov 11, 2006 . As this eMedTV article explains, a woman with Turner syndrome may have X chromosome monosomy, which is when there is an absence of .
http://genetics.emedtv.com/turner-syndrome/x-chromosome-monosomy.html

Orphanet Journal of Rare Diseases | Full text | Monosomy 18p
Monosomy 18p refers to a chromosomal disorder resulting from the deletion of all or part of the short arm of chromosome 18. The incidence is estimated to be .
http://www.ojrd.com/content/3/1/4