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Health Information Non-Traditional Inheritance

Non-Traditional Inheritance

Inheritance patterns which do not fall into the chromosomal, single gene, or multifactorial categories, are referred to as “non-traditional.” Listed in the directory below are some examples, for which we have provided a brief overview.

If you cannot find the information in which you are interested, please visit the Medical Genetics Online Resources page in this Web site for an Internet/World Wide Web address that may contain additional information on that topic.


Genetic Testing and Counseling
at Rush

The Section of Genetics at Rush University Medical Center in Chicago, Illinois, provides a full range of services for the diagnosis, counseling and treatment of patients (infants, children, adults and pregnant women) who have or are concerned about genetic and congenital disorders.

At Rush, physicians from more than 30 specialties address the full range of pediatric diseases and congenital problems, from the common to the complex. Rush pediatricians, pediatric surgeons, nurses and other health professionals provide care that aims to fulfill community needs, empower parents and advance pediatric care.

For more information about the genetic testing and counseling at Rush visit the Genetic Diagnosing and Counseling home page.

Or phone (888) RUSH-KID or (888) 787-4543.

Looking for More Health Information?

  • Visit our Health Information home page.
     
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  • Visit Discover Rush’s Web Resource page to find articles on health topics and recent health news from Rush University Medical Center in Chicago, Illinois. You will also find many helpful links to other areas of our site.

Looking for a Doctor?

Rush University Medical Center in Chicago, Illinois, is a leader in caring for people of all ages, from newborns through older adults.

Just phone (888) 352-RUSH or (888) 352-7874 for help finding the Rush doctor who’s right for you.


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Health Information Home
Medical Genetics Home Page
Non-Traditional Inheritance
Mitochondrial Inheritance: Leber's Optic Atrophy
Trinucleotide Repeats: Fragile-X Syndrome
Uniparental Disomy: Prader-Willi Syndrome, Angelman Syndrome

   
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