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Translocation Breakpoint

The point on a chromosome where the normal DNA sequence is juxtaposed with DNA from another chromosome. Usually expressed as a band number… Expand
National Institutes of Health

Papers overview

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Highly Cited
2011
Highly Cited
2011
Down syndrome (DS) is the most frequent genetic disorder leading to intellectual disabilities and is caused by three copies of… Expand
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Highly Cited
2011
Highly Cited
2011
Chromosomal translocations arise from the misjoining of DNA breaks, but the identity of the DNA repair factors and activities… Expand
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Highly Cited
2009
Highly Cited
2009
Purpose: Ewing sarcoma is an aggressive sarcoma and is the second most common bone sarcoma in childhood. Disease-specific t(11;22… Expand
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Review
2006
Review
2006
Recurring chromosome abnormalities are strongly associated with certain subtypes of leukemia, lymphoma and sarcomas. More… Expand
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Highly Cited
2002
Highly Cited
2002
We report here the identification and characterization of a novel gene (AUTS2) that spans the 7q11.2 breakpoint in a monozygotic… Expand
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Highly Cited
2001
Highly Cited
2001
Individuals affected with developmental disorders of speech and language have substantial difficulty acquiring expressive and/or… Expand
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Highly Cited
2001
Highly Cited
2001
Translocation t(15;19)(q13;p13.1) defines a lethal midline carcinoma arising adjacent to respiratory tract in young people. To… Expand
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Highly Cited
1996
Highly Cited
1996
A 200-300 kb region of chromosome 3p14.2, including the fragile site locus FRA3B, is homozygously deleted in multiple tumor… Expand
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Highly Cited
1992
Highly Cited
1992
Some acute lymphocytic leukaemias, particularly those in young children, are associated with a t(4;11)(q21;q23) reciprocal… Expand
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Highly Cited
1990
Highly Cited
1990
Three new neurofibromatosis type 1 (NF1) mutations have been detected and characterized. Pulsed-field gel and Southern blot… Expand
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