[HTML][HTML] Clinical, molecular and cytogenetic analysis of 46, XX testicular disorder of sex development with SRY-positive
QY Wu, N Li, WW Li, TF Li, C Zhang, YX Cui, XY Xia… - BMC urology, 2014 - Springer
Background To review the possible mechanisms proposed to explain the etiology of 46, XX
sex reversal by investigating the clinical characteristics and their relationships with …
sex reversal by investigating the clinical characteristics and their relationships with …
[HTML][HTML] 46,XX testicular disorder of sexual development with SRY-negative caused by some unidentified mechanisms: a case report and review of the literature
TF Li, QY Wu, C Zhang, WW Li, Q Zhou, WJ Jiang… - BMC urology, 2014 - Springer
Background 46, XX testicular disorder of sex development is a rare genetic syndrome,
characterized by a complete or partial mismatch between genetic sex and phenotypic sex …
characterized by a complete or partial mismatch between genetic sex and phenotypic sex …
Clinical, cytogenetic, and molecular analysis with 46, XX male sex reversal syndrome
X Gao, G Chen, J Huang, Q Bai, N Zhao… - Journal of assisted …, 2013 - Springer
Purpose To investigate the clinical characteristics of different categories of sex-reversed 46,
XX individuals and their relationships with chromosomal karyotype and the SRY gene …
XX individuals and their relationships with chromosomal karyotype and the SRY gene …
[HTML][HTML] Ten cases with 46, XX testicular disorder of sex development: single center experience
EC Akinsal, N Baydilli, A Demirtas, C Saatci… - International braz j …, 2017 - SciELO Brasil
Objective To present clinical, chromosomal and hormonal features of ten cases with SRY-
positive 46, XX testicular disorder of sex development who were admitted to our infertility …
positive 46, XX testicular disorder of sex development who were admitted to our infertility …
Two males with SRY-positive 46, XX testicular disorder of sex development
The 46, XX testicular disorder of sex development (46, XX testicular DSD) is a rare
phenotype associated with disorder of the sex chromosomes. We describe the clinical …
phenotype associated with disorder of the sex chromosomes. We describe the clinical …
[PDF][PDF] 46, XX male disorder of sexual development: a case report
The main factor influencing sex determination of an embryo is the sex-determining region Y
(SRY), a master regulatory gene located on the Y chromosome. The presence of SRY …
(SRY), a master regulatory gene located on the Y chromosome. The presence of SRY …
A novel mutation (c. 341A> G) in the SRY gene in a 46, XY female patient with gonadal dysgenesis
Z Helszer, A Dmochowska, J Szemraj… - Gene, 2013 - Elsevier
SRY (sex-determining region Y) gene, MIM 480000, NM_005634) is crucial for sex
differentiation which encodes the protein responsible for initiating testis differentiation. SRY …
differentiation which encodes the protein responsible for initiating testis differentiation. SRY …
SRY-negative 46,XX male with normal genitals, complete masculinization and infertility
S Rajender, V Rajani, NJ Gupta… - MHR: Basic science …, 2006 - academic.oup.com
XX maleness is a rare syndrome with a frequency of 1 in 20 000–25 000 males. XX males
exist in different clinical categories with ambiguous genitalia or partially to fully mature male …
exist in different clinical categories with ambiguous genitalia or partially to fully mature male …
XX Maleness and XX True Hermaphroditism in SRY-Negative Monozygotic Twins: Additional Evidence for a Common Origin
AT Maciel-Guerra, MP de Mello, FB Coeli… - The Journal of …, 2008 - academic.oup.com
Context: Differentiation of testicular tissue in 46, XX individuals is seen either in XX males,
the majority of them with SRY gene, or in individuals, usually SRY (−), with ovotesticular …
the majority of them with SRY gene, or in individuals, usually SRY (−), with ovotesticular …
[HTML][HTML] A 46, XX SRY-negative man with complete virilization and infertility as the main anomaly
A Valetto, V Bertini, E Rapalini, P Simi - Fertility and sterility, 2005 - Elsevier
OBJECTIVE: To report a case of a 46, XX SRY-negative man with a male phenotype and
azoospermia. DESIGN: Case report. SETTING: Molecular and Cytogenetic Unit in a …
azoospermia. DESIGN: Case report. SETTING: Molecular and Cytogenetic Unit in a …