ATYPICAL TRUE HERMAPHRODITISM WITH A MOSAIC 45,X/46,X,dic(Y) (q11.2) KARYOTYPE
Author:
Affiliation:
1. From the Departments of Urology and Geriatric Medicine, Akita University School of Medicine, Akita, Japan
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Urology
Reference3 articles.
1. Ambiguous genitalia in an elderly woman with a mosaic 45,X/46,X,dic(Y) (Q11.2) karyotype;Smith;Urology,1996
2. Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature;Tuck-Muller;Hum. Genet.,1995
3. Gonadal tumors in disorders of sexual differentiation;Gourlay;Urology,1994
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1. Cytogenetic Spectrum of Ovotesticular Difference of Sex Development (OT DSD) among a Large Cohort of DSD Patients and Literature Review;Sexual Development;2019
2. A Rare Mosaic Karyotype of 45,X/46,X,psu idic(Y)(p11.32)/46,XY with SHOX Haploinsufficiency, External Male Genitalia, and Short Stature;Sexual Development;2018-12-01
3. 45,X/46,XY ovotesticular disorder of sex development revisited: undifferentiated gonadal tissue may be mistaken as ovarian tissue;Journal of Pediatric Endocrinology and Metabolism;2017-01-01
4. Hypospadias in a male infant with an unusual mosaic 45,X/46,X,psu idic(Y)(p11.32)/46,XY and haploinsufficiency of SHOX: A case report;Molecular Medicine Reports;2017-01
5. Perspectives in Pediatric Pathology, Chapter 7. Ovotesticular DSD (True Hermaphroditism);Pediatric and Developmental Pathology;2015-09
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