Science > Abortion > Re: The moronity of the Jews is in their belief that they can fool all the world all the time
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Science > Abortion |
| User: |
"The Reverddd" |
| Date: |
04 Dec 2006 11:47:43 PM |
| Object: |
Re: The moronity of the Jews is in their belief that they can fool all the world all the time |
On 4 Dec 2006 21:19:22 -0800, "Sentinel" <unlearn34@yahoo.com> wrote:
Prime Minister of the Kingdom of God wrote:
The moronity of the Jews is in their belief that they can fool all the
world all the time
"The Jews", you said. The Jews are a people who are as different
from each other as americans are a mix of nationalities, ideologies
and religions. You speak as if they think in a cohesive unit, that
they
are all the same. The sign of a bigot is one who cannot tell the
difference between people of the same race.
The jew race is known for its genetic character defects.
.
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| User: "Harry" |
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| Title: Re: The moronity of the Jews is in their belief that they can fool all the world all the time |
05 Dec 2006 11:59:59 AM |
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"The Re'ver'ddd" <rennigade@angglkkkoon.com.za> wrote in message
news:457507d6.4214780@news.onetel.net.uk...
On 4 Dec 2006 21:19:22 -0800, "Sentinel" <unlearn34@yahoo.com> wrote:
Prime Minister of the Kingdom of God wrote:
The moronity of the Jews is in their belief that they can fool all the
world all the time
"The Jews", you said. The Jews are a people who are as different
from each other as americans are a mix of nationalities, ideologies
and religions. You speak as if they think in a cohesive unit, that
they
are all the same. The sign of a bigot is one who cannot tell the
difference between people of the same race.
The jew race is known for its genetic character defects.
Isn't what they said about your parents before they allowed your dad to *****
his sister?
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| User: "The Reverdnd" |
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| Title: Re: The moronity of the Jews is in their belief that they can fool all the world all the time |
05 Dec 2006 02:28:01 PM |
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On Tue, 5 Dec 2006 17:59:59 -0000, "Harry" <harry@leavemealone.com>
wrote:
"The Re'ver'ddd" <rennigade@angglkkkoon.com.za> wrote in message
news:457507d6.4214780@news.onetel.net.uk...
On 4 Dec 2006 21:19:22 -0800, "Sentinel" <unlearn34@yahoo.com> wrote:
Prime Minister of the Kingdom of God wrote:
The moronity of the Jews is in their belief that they can fool all the
world all the time
"The Jews", you said. The Jews are a people who are as different
from each other as americans are a mix of nationalities, ideologies
and religions. You speak as if they think in a cohesive unit, that
they
are all the same. The sign of a bigot is one who cannot tell the
difference between people of the same race.
The jew race is known for its genetic character defects.
Isn't what they said about your parents before they allowed your dad to *****
his sister?
No, it's what they said about yours as they led them to the showers.
TAXEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEE!!!!!!
.
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| User: "Benyamin Cramer" |
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| Title: Re: The moronity of the Jews is in their belief that they can fool all the world all the time |
05 Dec 2006 01:27:00 AM |
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This is a multi-part message in MIME format.
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"The Re'ver'ddd" <rennigade@angglkkkoon.com.za> wrote in message
news:457507d6.4214780@news.onetel.net.uk...
On 4 Dec 2006 21:19:22 -0800, "Sentinel" <unlearn34@yahoo.com> wrote:
Prime Minister of the Kingdom of God wrote:
The moronity of the Jews is in their belief that they can fool all the
world all the time
"The Jews", you said. The Jews are a people who are as different
from each other as americans are a mix of nationalities, ideologies
and religions. You speak as if they think in a cohesive unit, that
they
are all the same. The sign of a bigot is one who cannot tell the
difference between people of the same race.
The jew race is known for its genetic character defects.
Ken Oath. Here are a few
Ashkenazi Jewish Panel
When turnaround time matters most
Benefits
.
Fastest turnaround time in the industry - approximately two weeks
compared to up to five weeks for other laboratories
.
Minimal specimen volume required
.
Comprehensive, informative report
Clinical Summary
This Ashkenazi Jewish Panel detects mutations associated with the following
eight disorders that commonly occur in Ashkenazi-Jewish (Eastern European
Jewish) individuals:
.
Bloom syndrome
.
Canavan disease
.
Cystic fibrosis
.
Familial dysautonomia
.
Fanconi anemia group C
.
Gaucher disease
.
Niemann-Pick disease types A and B
.
Tay-Sachs disease
The panel simplifies test ordering for Ashkenazi Jewish individuals who wish
to know their carrier status and/or their risk of having a child with any of
these disorders. It is most frequently used for Ashkenazi Jews and their
partners who are pregnant or contemplating pregnancy. Since all of these
disorders are autosomal recessive, both parents must be carriers for the
couple to have an affected child. If one partner is Ashkenazi-Jewish and the
other is not, sequential screening, beginning with the Ashkenazi Jew, is
recommended.
Carrier Frequency and Detection Rate in the Ashkenazi-Jewish
Population
Disease
Carrier
Frequency
Number of Mutations Detected
Carrier Detection Rate (%)
Bloom syndrome
1 in 100
1
97
Canavan disease
1 in 40
4
99
Cystic fibrosis
1 in 25
25
97
Familial dysautonomia
1 in 30
1
98
Fanconi anemia group C
1 in 89
1
99
Gaucher disease
1 in 13
4
96
Niemann-Pick disease
type A: 1 in 90
4
96
type B: Unknown
4
95
Tay-Sachs disease
1 in 30
3
98
Quest Diagnostics Genetics Center
Physicians, if you need assistance with any genetic test, the Quest
Diagnostics Genetics Center is ready to assist you. A dedicated genetics
customer service professional will answer your question or, if appropriate,
connect you with one of our:
.
Seventeen directors certified by the American Board of Medical
Genetics,
.
Eight genetic counselors certified by the American Board of Genetic
Counseling, or
.
Two academic associates who are thought leaders from academic medical
centers.
Contact the Genetics Center toll-free, at 1-866-GENE-INFO (1-866-436-3463).
Our technical experts will be glad to assist you.
Online Resources for Healthcare Professionals
.
Obtain test ordering codes and specimen requirements from our online
Test Menu.
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Learn about genetic test selection, utilization, and interpretation in
our Interpretive Guide.
.
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solutions.
.
Learn more about our genetic testing capabilities.
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Read "Genomics meets reality" from the Quest Diagnostics Physician's
Update Newsletter, Winter 2002. This article discusses use of genetic
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Online Test Information for Your Patients
.
Our patient brochure for carrier screening in the Ashkenazi Jewish
population is available in both English and Russian. To obtain a supply of
these brochures for your office, contact your Quest Diagnostics sales
representative.
.
Your patients can learn about health conditions and laboratory tests in
our online Patient Health Library. The library is founded on evidence-based
information, and includes topics such as:
-
Bloom Syndrome
-
Canavan's Leukodystrophy
-
Familial Dysautonomia
-
Fanconi's Anemia
-
Gaucher Disease
-
Niemann Pick Disease
-
Tay-Sachs Disease
-
Genetic Testing
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Ask-the-Doctor Checklist
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Work in Partnership with Your Doctor
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Making Wise Health Decisions
The Disorders
.
Bloom syndrome: Children with Bloom syndrome are affected with growth
retardation, abnormalities in skin pigmentation, immunodeficiency, a
predisposition to cancer, and chromosomal instability. Death usually occurs
in the teens or twenties, most often caused by cancer.
.
Canavan disease: Canavan disease (aspartoacylase deficiency) is a
progressive neurologic disease characterized by increased head
circumference, decreasing muscle tone and motor activity, progressive loss
of visual responsiveness, and mental retardation. Death usually occurs by
age four.
.
Cystic fibrosis: Characteristic manifestations include recurrent lung
infections, malabsorption, malnutrition, and infertility (especially in
males). Median survival is 30 years.
.
Familial dysautonomia: Familial dysautonomia is characterized by
abnormal functioning of the sensory and autonomic nervous systems. This
causes decreased sensitivity to pain, abnormal regulation of body
temperature, paroxysmal hypertension, and gastrointestinal abnormalities.
.
Fanconi anemia group C: Fanconi anemia is characterized by deficient
bone development and bone marrow function. This can lead to pancytopenia,
anemia, leukemia, and malformations of the limbs, kidneys, and heart. The
disorder may be mild or severe.
.
Gaucher disease: Gaucher disease is a lysosomal glycolipid storage
disorder caused by an enzymatic deficiency (acid beta galactosidase
deficiency). Individuals may have an enlarged liver and spleen,
thrombocytopenia, anemia, bone pain, bone lesions, and fractures. Life
expectancy depends on severity of the symptoms.
.
Niemann-Pick disease types A and B: This lysosomal storage disorder is
characterized by diminished acid sphingomyelinase activity. Type A is
usually fatal within 2 to 3 years. These children fail to thrive, have an
enlarged liver and spleen, and exhibit progressive mental and physical
degeneration. Individuals with type B also have hepatosplenomegaly (along
with cirrhosis, portal hypertension, ascites, and pancytopenia), but little
to no neurologic involvement. They often survive into adolescence and
adulthood.
.
Tay-Sachs disease: Tay-Sachs is a progressive, neurodegenerative
disorder caused by an enzymatic deficiency (hexosaminidase A). The classic
infantile form is characterized by developmental retardation followed by
paralysis, dementia, seizures, and blindness. Death usually occurs by age 4.
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