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A human Y-chromosomal DNA sequence expressed in testicular tissueEvidence for distinguishable transcripts of the putative testis determining gene (ZFY) and mapping of homologous cDNA sequences to chromosomes X,Y and 9Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin YHigh mutation rates have driven extensive structural polymorphism among human Y chromosomesY chromosome specific probes identify breakpoint in a 45,X/46,X,del(Y)(pter----q11.1:) karyotype of an infertile male.Use of probes for ZFY, SRY, and the Y pseudoautosomal boundary in XX males, XX true hermaphrodites, and an XY female.An autosomal or X linked mutation results in true hermaphrodites and 46,XX males in the same familyExchange of terminal portions of X- and Y-chromosomal short arms in human XY femalesIsolation of a sequence which maps close to the human sex determining geneAbnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY females.Evolution of homologous sequences on the human X and Y chromosomes, outside of the meiotic pairing segment.Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes.Prenatal diagnosis of a 45,X male with a SRY-bearing chromosome 21.Is zinc-finger Y the sex-determining gene?An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunction.Steroid sulfatase gene in XX males.XX true hermaphroditism in southern African blacks: an enigma of primary sexual differentiationAn extended long-range restriction map of the human sex-determining region on Yp, including ZFY, finds marked homology on Xp and no detectable Y sequences in an XX male.Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency).MSY Breakpoint Mapper, a database of sequence-tagged sites useful in defining naturally occurring deletions in the human Y chromosome.Primary infertility in a phenotypic male with 46XX chromosomal constitutionAnalysis of sex chromosome abnormalities using X and Y chromosome DNA tiling path arrays.Intrachromosomal homologous recombination between inverted amplicons on opposing Y-chromosome arms.Dynamic nature of the proximal AZFc region of the human Y chromosome: multiple independent deletion and duplication events revealed by microsatellite analysis.XY sex reversal associated with a deletion 5' to the SRY "HMG box" in the testis-determining regionLoss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination.Clinical management issues in males with sex chromosomal mosaicism and discordant phenotype/sex chromosomal patterns.Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA-sequences.
P2860
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P2860
description
1986 nî lūn-bûn
@nan
1986 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1986 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
name
Variable transfer of Y-specific sequences in XX males.
@en
type
label
Variable transfer of Y-specific sequences in XX males.
@en
prefLabel
Variable transfer of Y-specific sequences in XX males.
@en
P2093
P2860
P356
P1476
Variable transfer of Y-specific sequences in XX males.
@en
P2093
Ferguson-Smith MA
Florentin L
Jamieson D
Mitchell M
P2860
P304
P356
10.1093/NAR/14.13.5375
P407
P577
1986-07-01T00:00:00Z