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Y chromosome deletions

Known as: Partial deletion of Y, Y chromosome deletion, Partial deletion of chromosome Y 
 
National Institutes of Health

Papers overview

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2014
2014
The azoospermia factor (AZF) region of the human Y chromosome contains essential genes for spermatogenesis. Microdeletions in AZF… Expand
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2013
2013
NRXN1 microdeletions occur at a relatively high frequency and confer increased risk for neurodevelopmental and neurobehavioral… Expand
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2013
2013
PurposeYq microdeletions are the leading genetic cause of male infertility and its detection is clinically relevant for… Expand
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2011
2011
The overgrowth disorder Beckwith–Wiedemann syndrome (BWS) is associated with dysregulation of imprinted genes at chromosome 11p15… Expand
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2010
2010
PurposesTo investigate the frequencies of AZF microdeletions and chromosomal abnormalities in infertile men from Northeastern… Expand
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Highly Cited
2007
Highly Cited
2007
CONTEXT An explosive growth in Y chromosome long arm (Yq) microdeletion testing demand for male infertility occurred in the past… Expand
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2007
2007
AIM To evaluate for the first time the frequency of Y chromosome microdeletions and the occurrence of the partial deletions of… Expand
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2001
2001
Deletions of the azoospermia factors on the Y chromosome long arm are an important cause of male infertility, and they may… Expand
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Highly Cited
1999
Highly Cited
1999
To clarify whether cryptorchidism might be the expression of an intrinsic congenital testicular abnormality, we investigated the… Expand
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Highly Cited
1998
Highly Cited
1998
Idiopathic Sertoli cell-only syndrome (SCOS) is characterized by azoospermia, small testes, absence of germ cells in the testes… Expand
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