A unique clonal chromosome 2 deletion in endomyometriosis
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This paper describes a unique clonal deletion on chromosome 2 identified in patients with endomyometriosis.
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References (17)
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- ETIOLOGY, PREVENTION, AND INHIBITION OF ENDOMETRIOSIS via openalex
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Cited by (5)
- Clinicopathological Characteristics of Primary Ovarian Adenomyoma: A Single-institutional Experience 2017
- Hepatic Uterus-Like Mass Misdiagnosed as Hepatic Abscess 2014
- Uterus‐like mass: MRI appearance of a very rare entity 2007
- Endomyometriosis arising in the uterosacral ligament: A case report including a literature review and immunohistochemical analysis 2000
- Expression pattern of integrin adhesion molecules in endometriosis and human endometrium 1998
Source provenance
- europepmc
- last seen: 2026-06-04T01:30:01.192114+00:00
- openalex
- last seen: 2026-06-04T00:00:01.174412+00:00
- unpaywall
- last seen: 2026-06-02T02:00:03.124865+00:00
License: CC0
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