XX maleness is the most common condition in which testes develop in the absence of a cytogenetically detectable Y chromosome. Using molecular techniques, it is possible to detect Yp sequences in the majority of XX males. In this study, we could detect Y-specific sequences, including the sex-determining region of the Y chromosome (SRY), using fluorescence in situ hybridization. In 5 out of 6 previously unpublished XX males, SRY was translocated onto the terminal part of an X chromosome. This is the first report in which translocation of an SRY-bearing fragment to an X chromosome in XX males could be directly demonstrated. © 1992 Springer-Verlag.SCOPUS: ar.jinfo:eu-repo/semantics/publishe
The main factor influencing sex determination of an embryo is the sex-determining region Y (SRY), a ...
Cytogenetic studies on an azoospermic male revealed a balanced Y;1 translocation: 46,X,t(Y;1)(q12;p3...
Cytogenetic studies on an azoospermic male revealed a balanced Y;1 translocation: 46,X,t(Y;1)(q12;p3...
XX maleness is the most common condition in which testes develop in the absence of a cytogenetically...
XX maleness is the most common condition in which testes develop in the absence of a cytogenetically...
We investigated the presence of Y-material in the genome of an azoospermic male with 46,XX karyotype...
Cytogenetic analysis, fluorescent in situ hybridisation (FISH), and molecular am-plification have be...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/71879/1/j.1749-6632.1987.tb25088.x.pd
Isochromosome Y is one of the structural anomalies of the Y chromosome associated with a 45,X cell l...
Background/PurposeXX male is a rare sex chromosomal disorder in infertile men. The purpose of this s...
For the purposes of this study, several panels were constructed, the majority of effort and time foc...
Copyright © 2008 John Wiley & SonsAims: To evaluate fluorescence in situ hybridization (FISH) for SR...
To determine if human XX maleness results from an abnormal chromosomal X-Y interchange, we studied t...
XX male is a rare sex chromosomal disorder in infertile men. The purpose of this study was to distin...
BACKGROUND: SRY (sex-determining region, Y) is the gene responsible of gonadal differentiation in th...
The main factor influencing sex determination of an embryo is the sex-determining region Y (SRY), a ...
Cytogenetic studies on an azoospermic male revealed a balanced Y;1 translocation: 46,X,t(Y;1)(q12;p3...
Cytogenetic studies on an azoospermic male revealed a balanced Y;1 translocation: 46,X,t(Y;1)(q12;p3...
XX maleness is the most common condition in which testes develop in the absence of a cytogenetically...
XX maleness is the most common condition in which testes develop in the absence of a cytogenetically...
We investigated the presence of Y-material in the genome of an azoospermic male with 46,XX karyotype...
Cytogenetic analysis, fluorescent in situ hybridisation (FISH), and molecular am-plification have be...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/71879/1/j.1749-6632.1987.tb25088.x.pd
Isochromosome Y is one of the structural anomalies of the Y chromosome associated with a 45,X cell l...
Background/PurposeXX male is a rare sex chromosomal disorder in infertile men. The purpose of this s...
For the purposes of this study, several panels were constructed, the majority of effort and time foc...
Copyright © 2008 John Wiley & SonsAims: To evaluate fluorescence in situ hybridization (FISH) for SR...
To determine if human XX maleness results from an abnormal chromosomal X-Y interchange, we studied t...
XX male is a rare sex chromosomal disorder in infertile men. The purpose of this study was to distin...
BACKGROUND: SRY (sex-determining region, Y) is the gene responsible of gonadal differentiation in th...
The main factor influencing sex determination of an embryo is the sex-determining region Y (SRY), a ...
Cytogenetic studies on an azoospermic male revealed a balanced Y;1 translocation: 46,X,t(Y;1)(q12;p3...
Cytogenetic studies on an azoospermic male revealed a balanced Y;1 translocation: 46,X,t(Y;1)(q12;p3...