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10q22

A chromosome band present on 10q
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
The inflammatory bowel diseases (IBD) Crohn's disease and ulcerative colitis are common causes of morbidity in children and young… Expand
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Highly Cited
2005
Highly Cited
2005
Preeclampsia is a pregnancy-associated disease with maternal symptoms but placental origin. Epigenetic inheritance is involved in… Expand
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Highly Cited
2005
Highly Cited
2005
The large conductance calcium-sensitive potassium (BK) channel is widely expressed in many organs and tissues, but its in vivo… Expand
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Highly Cited
2001
Highly Cited
2001
DNA sequence amplifications are involved in the progression of many tumor types, and have also been found in advanced prostate… Expand
Highly Cited
2000
Highly Cited
2000
  • C. Eng
  • Journal of medical genetics
  • 2000
  • Corpus ID: 27076421
Cowden syndrome (CS, MIM 158350) is an autosomal dominant disorder with age related penetrance characterised by multiple… Expand
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Review
2000
Review
2000
  • P. Dahia
  • Endocrine-related cancer
  • 2000
  • Corpus ID: 27405328
For many years, it has been thought that the chromosome region 10q22-24 includes one or more genes that appear to play a role in… Expand
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Highly Cited
1999
Highly Cited
1999
Germline mutations in PTEN, encoding a dual-specificity phosphatase on 10q23.3, cause Cowden syndrome (CS), which is… Expand
Highly Cited
1997
Highly Cited
1997
Cowden disease, also known as multiple hamartoma syndrome, is an autosomal dominant cancer syndrome with a high risk of breast… Expand
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Highly Cited
1997
Highly Cited
1997
The majority of familial medullary thyroid neoplasms are associated with germ-line mutations of the RET proto-oncogene, yet very… Expand
Highly Cited
1994
Highly Cited
1994
Karyotypic and molecular data indicate that genetic events involving the chromosome region 10q22-10qter may be related to… Expand
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