chromosome microdeletions are the most frequent genetic cause of severe oligozoospermia (,5 million spermatozoa/ml) and azoospermia (absence of sperma-tozoa in the ejaculate).1 Microdeletions associated with infertility occur in specific regions of the long arm of the Y chromosome, called azoospermia factor (AZF) regions.2 3 In 1996, three types of AZF deletion (AZFa, AZFb, and AZFc) were described by Vogt et al; however, after the complete physical map and sequence of the AZFb and AZFc regions was produced,4 it became evident that the AZFb and AZFc intervals partially overlap.5 The Y chromosome is extremely rich in repetitive sequences, organised in amplicons.6 Ampliconic sequences are characterised by sequence pairs showing nearly complet...
Purpose: To determine the relationships between idiopathic oligo- or azoospermia and microdeletions ...
Background: In some cases infertile men showed small deletions of specific genes in the Y chromosome...
Human chromosome deletions in Yq11 seem to occur frequently as de novo mutation events in men with i...
The Y chromosome carries several spermatogenesis genes distributed in three regions: AZFa, AZFb and ...
Background & Aims: The most significant cause of infertility in men is the genetic deletion in the a...
Abstract The human Y chromosome harbors genes that are responsible for testis development and also f...
BACKGROUND: Y chromosome microdeletions are associated with severe male factor infertility. In this ...
According to the latest data, globally 15% of couples have infertility and male infertility contribu...
Microdeletions in azoospermia factor (AZF) region on distal Yq are associated with male infertility ...
The spermatogenesis failure with a genetic defect is one of the major causes of male infertility. Th...
After the Klinefelter syndrome, Y chromosome microdeletions are the second most frequent genetic cau...
Due to globally increasing problem of infertility and its effect in the life of affected couple’s, i...
Male infertility represents around half of all cases of infertility. The microdeletions of the azoos...
BACKGROUND: Complete deletions of the AZFc region in distal Yq are the most frequent molecular gene...
Background: Chromosomal abnormalities and Y chromosome microdeletions are re-garded as two most freq...
Purpose: To determine the relationships between idiopathic oligo- or azoospermia and microdeletions ...
Background: In some cases infertile men showed small deletions of specific genes in the Y chromosome...
Human chromosome deletions in Yq11 seem to occur frequently as de novo mutation events in men with i...
The Y chromosome carries several spermatogenesis genes distributed in three regions: AZFa, AZFb and ...
Background & Aims: The most significant cause of infertility in men is the genetic deletion in the a...
Abstract The human Y chromosome harbors genes that are responsible for testis development and also f...
BACKGROUND: Y chromosome microdeletions are associated with severe male factor infertility. In this ...
According to the latest data, globally 15% of couples have infertility and male infertility contribu...
Microdeletions in azoospermia factor (AZF) region on distal Yq are associated with male infertility ...
The spermatogenesis failure with a genetic defect is one of the major causes of male infertility. Th...
After the Klinefelter syndrome, Y chromosome microdeletions are the second most frequent genetic cau...
Due to globally increasing problem of infertility and its effect in the life of affected couple’s, i...
Male infertility represents around half of all cases of infertility. The microdeletions of the azoos...
BACKGROUND: Complete deletions of the AZFc region in distal Yq are the most frequent molecular gene...
Background: Chromosomal abnormalities and Y chromosome microdeletions are re-garded as two most freq...
Purpose: To determine the relationships between idiopathic oligo- or azoospermia and microdeletions ...
Background: In some cases infertile men showed small deletions of specific genes in the Y chromosome...
Human chromosome deletions in Yq11 seem to occur frequently as de novo mutation events in men with i...