X-Y chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome
No abstract listed.
The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditism
Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesis
Investigation of three XX males by cytogenetic and DNA analyses. Suggestion of Y chromosome inversion polymorphism
Further cytologic evidence for Xp-Yp translocation in XX males using in situ hybridization with Y-derived probe
Meiosis in Sxr male mice: II. Further absence of cytological evidence for a Y-autosome rearrangement in sex-reversed (Sxr) mice
Immunocytochemical labelling of the kinetochore of human synaptonemal complexes, and the extent of pairing of the X and Y chromosomes
Evidence of a preferential inactivation of the paternally derived X chromosome in a 46,XX true hermaphrodite
Familial true hermaphrodism in three siblings: clinical, cytogenetic, histological and hormonal studies
Candidate genes in complete and partial XY sex reversal: mutation analysis of SRY, SRY-related genes and FTZ-F1
Early manifestations of testicular dysgenesis in children: pathological phenotypes, karyotype correlations and precursor stages of tumour development
Highly homologous loci on the X and Y chromosomes are hot-spots for ectopic recombinations leading to XX maleness
A theory of the origin of cerebral asymmetry: epigenetic variation superimposed on a fixed right-shift
A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm
Regional assignment of Y-linked DNA probes by deletion mapping and their homology with X-chromosome and autosomal sequences
Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency)
Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes
An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome
Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA-sequences
Recombination between the X and Y chromosomes: implications for the relationship between MIC2, XG and YG
X-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies
Use of probes for ZFY, SRY, and the Y pseudoautosomal boundary in XX males, XX true hermaphrodites, and an XY female
Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis
Perspectives in Pediatric Pathology, Chapter 16. Klinefelter Syndrome and Other Anomalies in X and Y Chromosomes. Clinical and Pathological Entities
Definitive evidence for the short arm of the Y chromosome associating with the X chromosome during miosis in the human male
Physical mapping of deletion breakpoints in patients with X-linked ichthyosis: evidence for clustering of distal and proximal breakpoints
A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif
Atypical XX male with the SRY gene located at the long arm of chromosome 1 and a 1qter microdeletion
Prenatal diagnosis of 46,XX testicular DSD. Molecular, cytogenetic, molecular-cytogenetic, and ultrasonographic evaluation
Combined Leydig cell and Sertoli cell dysfunction in 46,XX males lacking the sex determining region Y gene
Sex vesicle "entrapment": translocation or nonhomologous recombination of misaligned Yp and Xp as alternative mechanisms for abnormal inheritance of the sex-determining region
Rare rearrangements: a "jumping satellite" in one family and autosomal location of the SRY gene in an XX male
H-Y antigen studies in thirty patients with abnormal gonadal differentiation: correlations among sex chromosome complement, H-Y antigen, and gonadal type
Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blots
Hormonal and molecular genetic findings in 46,XX subjects with sexual ambiguity and testicular differentiation
Clinical, endocrinological, and epigenetic features of the 46,XX male syndrome, compared with 47,XXY Klinefelter patients
True hermaphroditism or gonadal intersexuality. Cytogenetic and gonadal analyses of 5 new examples related to 67 known cases studied cytogenetically
In situ fluorescence hybridization of Y translocations: cytogenetic analysis using probes Y190 and Y431
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