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Noonan syndrome - Symptoms and causes - Mayo Clinic Noonan syndrome is a genetic condition that stops typical development in various parts of the body It can affect a person in several ways, including unusual facial features, short height, heart problems and other physical problems
Noonan syndrome - Wikipedia Noonan syndrome (NS) is a genetic disorder that may present with mildly unusual facial features, short height, congenital heart disease, bleeding problems, and skeletal malformations [1]
Noonan Syndrome (Leopard Syndrome): Causes Outlook Noonan syndrome is a genetic condition that can affect many parts of your child’s body While symptoms vary widely, they most often include unusual facial features, short stature and heart problems
Noonan syndrome: MedlinePlus Genetics Noonan syndrome is a condition that affects many areas of the body It is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms
Noonan Syndrome Foundation | noonan syndrome What is Noonan Syndrome? Noonan syndrome can impact nearly every system in the body, causing heart defects, bleeding issues, developmental delays, and more Despite its prevalence, research is still uncovering its complexities
Noonan syndrome - UpToDate Noonan syndrome (NS) is a common autosomal-dominant condition that is associated with short stature and congenital heart disease (CHD), most often pulmonic stenosis
About Noonan Syndrome - National Human Genome Research Institute Noonan syndrome is a disorder that involves unusual facial characteristics, short stature, heart defects present at birth, bleeding problems, developmental delays, and malformations of the bones of the rib cage
Noonan Syndrome | Childrens Hospital of Philadelphia Noonan syndrome is a genetic disorder characterized by short stature, distinctive facial features, heart defects, bleeding problems, and skeletal abnormalities
What Is Noonan Syndrome? Does My Child Have the Signs? - WebMD Noonan syndrome is a rare genetic disorder If you have it, you might have certain identifiable facial features, short height, and unusual chest shape You may also have heart defects It can