1997
DOI: 10.1016/s0015-0282(97)80083-0
|View full text |Cite
|
Sign up to set email alerts
|

Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

1
17
0
1

Year Published

1998
1998
2023
2023

Publication Types

Select...
9
1

Relationship

0
10

Authors

Journals

citations
Cited by 180 publications
(19 citation statements)
references
References 22 publications
1
17
0
1
Order By: Relevance
“…A possible explanation for such variable phenotypes is the progressive germ cell regression over time, which has been reported in patients with AZFc deletions [3][4][5][6][7][8].…”
Section: Introductionmentioning
confidence: 99%
“…A possible explanation for such variable phenotypes is the progressive germ cell regression over time, which has been reported in patients with AZFc deletions [3][4][5][6][7][8].…”
Section: Introductionmentioning
confidence: 99%
“…It has been proposed that microdeletions of this region are probably responsible for testicular damage, leading to the development of undescended testis [19]. Moreover, patients with Y chromosome microdeletions and cryptorchidism have been reported in numerous studies [20][21][22][23][24]. However, there are studies reporting that there were no microdeletions in men with cryptorchidism [25].…”
Section: Introductionmentioning
confidence: 99%
“…Current practice is to screen for AZFa, P5/P1 and AZFc deletions, and some advocate screening for gr/gr deletions as well [39,40]. The presence of an AZFa or P5/P1 deletion indicates an extremely low chance of finding sperm during a testicular sperm extraction (TESE) procedure [29 ].…”
Section: Class Of Sequence Genementioning
confidence: 99%