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Y CHROMOSOME  

When your missing a chromosome, your missing alot.

An overview of the defect on chromosome 5 that may lead to the development of cancer, including colorectal cancer

While the exact cause and origin of DWS is not known, it is believed to affect chromosome 3, 9, 13 and 18 and lead to significant health complications in children.

G6PD deficiency creates blood disorders in children, thus a need for chromosome screening at birth.

Edwards' syndrome is a disease that is caused by a gene abnormality, where a person has a third copy of chromosome eighteen.

Offering an overview of the cause, origin, symptoms and management of adrenoleukodystrophy, a genetic disorder.

Should a woman preach and teach in the church? This debate has persisted for centuries. What ought women to do with their spiritual gifts? Would God give women teaching and preaching gifts, if He did not intend for them to use these talents for His glory?

Within moments of birth it is possible to tell if a baby may have Pallister Killian Syndrome. The advancement of genetics study has provided new, useful information.

This article discusses the inheritance of the Cystic Fibrosis gene and the symptoms, treatments and the global statistics of the disease.

Finally, scientists prove what women have known all along!

Down syndrome is a genetic disability that affects every race, nationality, and socioeconomic status.

This syndrome affects only males and is caused by the wrong number of chromosomes upsetting the natural balance of the body. This upset leads to a feminine body build (including breasts), underdevelopment of the testicles, and a taller than average height in adulthood.

The Y chromosome signals trouble when purchasing a cell phone.

Down syndrome is a chromosomal disorder in which there is an extra copy of chromosome 21 in the cells of the developing fetus. This article will explore the methods of diagnosing Down syndrome.

Offering an overview of Edwards' syndrome, a genetic disorder at chromosome 18

Rett's Syndrome is a genetic disorder that occurs on the X chromosome that most often occurs in females.

Von Hippel Lindau (VHL) is a chronic disorder found on chromosome three, the so-called "tumor suppressor gene" which logically means that tumors are more likely to grow. Unfortunately for me, VHL's also inherited, but that doesn't mean I'm doomed...

"We found that females in the hybrid zone develop a sexual preference for males belonging to their own species and that this preference is determined by genes located on the sex chromosome."

Muscular dystrophy is a degentic muscle disease caused by a genetic mutation within the X chromosome. At this time there is no cure and no known prevention.

My son Tommy has Angelman Syndrome, which is a rare genetic disorder due to a deletion of chromosome 15.

Everyday a mother somewhere is giving birth to a child with Down syndrome. It is a mistake in the chromosome formation, in which there is an extra 21st chromosome.

Down's syndrome is a genetic condtion that happens because of the presence of an extra chromosome. it was first described in 1886 and is not classed as a disease as childdren do not suffer from Down's syndrome.

According to the FDA, the treatment Tasigna (nilotinib) has been approved and released for use with Philadelphia chromosome positive chronic myeloid leukemia or CML.

New study shows that part of an abnormal chromosome is linked to colon cancer.

Men may become extinct one day, due to a ticking time bomb within their genes: the Y chromosome. Will this spell the end of humanity as we know it?

Down syndrome is a chromosomal disorder in which there is an extra copy of chromosome 21 in the cells of the developing fetus. This article will explore the various characteristics of people with Down syndrome.

Down syndrome is a chromosomal disorder in which there is an extra copy of chromosome 21 in the cells of the developing fetus. This article will explore myriad and varying needs of people with Down syndrome.

Down syndrome is a chromosomal disorder in which there is an extra copy of chromosome 21 in the cells of the developing fetus. This article will explore the three causes of Down syndrome.

This syndrome, which is the leading cause of mental retardation in males, is the result of overactive Cytosine-Guanine-Guanine nucleic acid production on a specific gene on the X chromosome.

One gene, "neurexin 1," and an area of chromosome 11 with another gene, were recently identified by The Autism Genome Project. Both were found in many of the families that participated.

Down syndrome is a chromosomal disorder in which there is an extra copy of chromosome 21 in the cells of the developing fetus. This article will explore many of the frequently asked questions (FAQ) about Down syndrome.

Down syndrome is a chromosomal disorder. As the result of an extra copy of chromosome 21 that the developing fetus possesses, the child with Down syndrome has physical, medical, and cognitive disorders which vary in severity from case to case.

Triple X syndrome is not inherited, but usually occurs as a random event during the formation of the reproductive cells. Triple-X syndrome is also known as Triplo X syndrome, Trisomy X, 47,XXX and XXX syndrome.

Down syndrome is a chromosomal disorder in which there is an extra copy of chromosome 21 in the cells of the developing fetus. What follows is an account of my very close relationship with someone with Down Syndrome.

Down syndrome is a genetic disease caused by three major factors, genetics, chromosome formation and cell division. Through scientific research, scientists have made vast discoveries on how to "treat" people with the disease.

Turner's Syndrome is an inherited, chromosome disorder that only affects females. The Internet is a good source of information about Turner's Syndrome and here are some good sites for those interested in finding out more…

Research on Cancer for undergraduate college.

As the leading cause of cardiac birth defect Noonan Syndrome is a condition for which many parents are unprepared. This is an overview of the Noonan Syndrome.

My daughter Noel was born with a rare neuro-genetic disorder called Angelman Syndrome. The most common question I am asked is “What is Angelman Syndrome?” This article is an attempt to give others a general overview of the disorder.

Each year, thousands of children are diagnosed with a Muscular Dystrophy condition. Of these children, many will suffer from the Duchenne subtype, often leading to rapid deterioration in the quality of life. This is an overview of Duchenne and its implication in children.

Leukemia. Most people have heard of it or maybe known somebody that has it. Now you should take the time to understand it.

The Earth and everything on it is evolving at a faster and faster rate, the Earth, the oceans, the climate, and even the people are evolving in order to adapt to the New Age that is quickly developing around us.

People are a constant source of inspiration.

there should be a limit on what people can do in the name of "having a good time."

Shwachman-Diamond Syndrome is a rare genetic syndrome that is often misdiagnosed. It is important for parents to know the signs and symptoms for the health of their child.

This disease is one of the diseases where knowledge of DNA can help us identify the disease early so that the victim can lead as normal a life as possible.

Sickle Cell Anemia is a genetic, hereditary disorder that affects the red blood cells of individuals. The internet can be a good place to find more information about Sickle Cell anemia. Here are some helpful sites online:

Are telomeres the key to the fountain of youth? They're more complicated than drinking from a mystical spring, but studies show they can prolong life.

New parents all envision their child to be a perfect little clone of themselves. But what happens when we learn that our little ones are going to have a lifetime of challenges ahead of them?

New hope on the medical front to identify and help treat this debilitating medical condition.

Rett Syndrome is a childhood neurodevelopment disorder. This is condition that almost exclusively occurs in females. It happens about once in every 10,000-15,000 live female births, and it is seen in all racial and ethnic groups worldwide.

Achondroplasia is the most common form of Dwarfism. It affects about one in every 25,000 births and it occurs in all races and in both sexes

Cystic Fibrosis is a genetic, potentially life-threatening lung disease. The internet has some great resources for those who'd like to find out more about cystic fibrosis:

How would you like to go through your entire life where your body is unable to control bleeding whether it is internal or external? My six year old cousin, Parker, as well as many other people in the world suffers from this every day of their lives.

Although I've been an avid viewer of the hit CBS television spin-off, CSI Miami, and thoroughly enjoy each character on the hit show, I had absolutely no idea that one of its stars, Khandi Alexander, actually made a huge name for herself in another venue.

Hemophilia is an incurable genetic disease in which a person's blood clots very slowly, or fails to clot at all. The Internet provides a great deal of information for those interested in finding out more about hemophilia.

Ever want to get some damn Myspace comments, but you don't know how? This is a simple guide to receiving comments on your Myspace page.

China is the fastest growing economic superpower in the world. India comes a close second. What is not widely known, however, is that these two powerhouses harbor a dark and sinister secret. When it comes to having children, boys are overwhelmingly the preferred sex.

A look at a kind of color blindness

U.S researchers had said Sunday a drug that has long been used to study epilepsy can help to improve learning in mice with a form of Down syndrome.

Know the facts on what you are putting in your body.

People with the condition have recently been featured on TLC. But what exactly is this condition, and what are the chances of passing it on? Read on to find out.

Prader-Willi Syndrome is a rare complex genetic disease. Individuals with this condition are always hungry.

When parents hear the news that their baby most likely will be born with DS, these parents go through many different emotions.

This paper will inform readers of the benefits studying behavioral genetics has for thousands of people with behavioral disorders. People with autism and dyslexia will be focused on specifically.

Think you're no longer a manly man when you get hitched? Try these heels on for size.

Who doesn't love watching someone get hurt? If you don't then you are some panty waste who is not truly human. And if you agree with both of the previous statements this is the article for you.

A self case study and clinical synopsis of a man afflicted with the neurological disability, Duchene's Muscular Dystrophy.

Analyzes the failure to reach a negotiated peace settlement in the Israeli-Palestinian conflict.

As an avid poker player and member of the Atlanta Poker Club (www.atlantapokerclub.com), I have developed a few suggested additions to the poker lexicon.

Fabry disease an inherit enzyme deficiency, accumulation of fat in blood vessels, leading to damaging various tissues, including heart & kidney. Genetically effects men & women differently. Fabrazyme enzyme replacement treatment.

It's been known for some time now that women and their unborn babies exchange cells. What hasn't been so clear is whether this is helpful or harmful. The research so far has been surprising.

The History of Autism has been both complex and controversial. Many people think that Autism is a modern disorder but as you have read it has dated back to the early 1800s.

Were you pressured by your doctor or genetic counselor to get an amnio? Did you and your mate agree upon the amnio procedure? Read about the amniosentesis test here and tell everyone what your opinion is!

As a general rule, colorblindness sufferers acquire the condition at birth. However, in some cases, colorblindness may be attributed to disease or medication. This is an overview.

Tests currently used to identify Down Syndrome can be risky, so researchers are developing more accurate ways to analyze blood. Their most recent efforts are very promising.

Always thought and/or heard that comics were just for kids? Well I say that is plain rubbish! Not everything out there consists of overly-muscled men in tights and anatomically-improbable women. Comics can be a thinking man's (or women's) game, too!

The new field of genetic genealogy is providing exciting new possibilities for genealogical research. This article gives you a basic understanding of what it is and the basics of how it works.

The first draft of the horse genome sequence has been deposited in public databases and is freely available to researchers.

DNA analysis can help family historians break through brick walls and uncover information on genetic disorders and disease.

AN UNDERGROUND TRANSIT System operated for twenty-four years through President, Calaveras, and Snohomish Counties without suffering a solitary mishap. The Regional Transit Authority's "Vision 2020" had been well realized.

Fluoride is everywhere ... toothpaste, drinking water, soups and countless other products. Why is it so ubiquitous ... is it really good for us? Perhaps not.

Trisomy 18 is a chromosomal abnormality occurring in 1 out of 3000 live births. Trisomy 18 is almost always fatal. Friends and family members need to be supportive in whatever choices the parents make in regards to the pregnancy.

This piece addresses pregnancy and parenting myths for women over 35.

A brief introduction to the Shettles Method, a way to determine whether you conceive a boy or girl.

Gel electrophoresis process uses a gel with DNA samples inserted into tiny wells at one end of the gel.

When both parents have type A blood, their child will have either type A or type O. Type O can occur when both parents have a genotype of AO.

What people don't understand about Down Syndrome and how the disorder is treated.

A brief description of common methods of determining the gender of your child, and resources for more information.

Approved in 1995 by the FDA, Losartan(Cozaar) has been used to treat hypertansion. Harry Dietz's team at JHMI has found that it can combat aortic anuerysms and aortic dissection, and can possibly eliminate the need for surgery in MFS patients.

This article offers myths and tips on how to conceive a baby boy. Make sure to talk to your doctor before attempting any "old wives tales" or "home remedies".

Fragile X Syndrome is the number one inherited reason for mental retardation and the only inherited disorder that can cause autism. One in every 259 women can be a carrier. Do you know if you are?

I had a friend who died of ovarian cancer a few years ago after a long battle, having beaten it five times with chemo.

Race is dead--so why do some say "long live race"? Is a race based medicine likely to save more (especially minority) lives? At what social costs? I address these and other questions in a end of term paper written in 2002.

At my initial leukemia diagnosis, I knew next to nothing and was terrified. Now I just want to share what I've learned with others who might someday find themself in that place. Here are the basics on leukemia. And for the record, it is survivable!

There are numerous ways that a fetus can develop intersexually, and most physicians can not confidently say that an infant was �meant' to be either male or female. The key question becomes a bloody one, to or not to use the scalpel...

There are many medical, physical and psychological issues that adopted toddlers may face, whether adopted domestically or from another country.

Beckwith-Wiedemann Syndrome is an extremely rare disease that most have never heard of and fortunately have never had to deal with.

Pregnancy discrimination is alive and well in today's work driven society. Get a first hand look at one of the most underhanded and yet most overlooked types of discrimination.

Nature versus Nurture has always been a hot topic in psychology when determining personality. Nature, being the genetic element of natural attributes, and nurture applying to environmental factors, and life experience.