Literature DB >> 3473936

A 45,X male with Y-specific DNA translocated onto chromosome 15.

A Gal, B Weber, G Neri, A Serra, U Müller, W Schempp, D C Page.   

Abstract

A 20-year-old male patient with chromosomal constitution 45,X, testes and normal external genitalia was examined. Neither mosaicism nor a structurally aberrant Y chromosome was observed when routine cytogenetic analysis was performed on both lymphocytes and skin fibroblasts. Y chromosome-specific single-copy and repeated DNA sequences were detected in the patient's genome by means of 11 different recombinant-DNA probes of known regional assignment on the human Y chromosome. Data indicated that the short arm, the centromere, and part of the long-arm euchromatin of the Y chromosome have been retained and that the patient lacks deletion intervals 6 and 7 of Yq. High-resolution analysis of prometaphase chromosomes revealed additional euchromatic material on the short arm of one of the patient's chromosomes 15. After in situ hybridization with the Y chromosome-specific probe pDP105, a significant grain accumulation was observed distal to 15p11.2, suggesting a Y/15 chromosomal translocation. We conclude that some 45,X males originate from Y-chromosome/autosome translocations following a break in the proximal long arm of the Y chromosome.

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Year:  1987        PMID: 3473936      PMCID: PMC1684161     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  34 in total

1.  Male with 45,X karyotype.

Authors:  A Forabosco; A Carratu; M Assuma; A De Pol; B Dutrillaux; E Cheli
Journal:  Clin Genet       Date:  1977-08       Impact factor: 4.438

2.  Mapping the locus of the H-Y gene on the human Y chromosome.

Authors:  G C Koo; S S Wachtel; K Krupen-Brown; L R Mittl; W R Breg; M Genel; I M Rosenthal; D S Borgaonkar; A D Miller; R Tantravahi; R R Schreck; B F Erlanger; O J Miller
Journal:  Science       Date:  1977-12-02       Impact factor: 47.728

3.  Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Authors:  L M Kunkel; K D Smith; S H Boyer; D S Borgaonkar; S S Wachtel; O J Miller; W R Breg; H W Jones; J M Rary
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

4.  New Giemsa method for the differential staining of sister chromatids.

Authors:  P Perry; S Wolff
Journal:  Nature       Date:  1974-09-13       Impact factor: 49.962

5.  Robertsonian translocation between the chromosome Y and 15.

Authors:  I Subrt; B Blehová
Journal:  Humangenetik       Date:  1974

6.  XO and male phenotype.

Authors:  F Lo Curto; E Pucci; S Scappaticci; S Scotta; F Severi; G R Burgio; M Fraccaro
Journal:  Am J Dis Child       Date:  1974-07

7.  Translocation Y/5 resulting in Cri du Chat syndrome.

Authors:  P Vignetti; L Chessa; L Bruni; E Ferrante; B Dallapiccola
Journal:  Clin Genet       Date:  1977-12       Impact factor: 4.438

8.  Cytogenetical and clinical investigations in four subjects with anomalies of sexual development.

Authors:  M Fraccaro; J Lindsten; H P Klinger; L Tiepolo; C G Bergstrand; K M Herrlin; A Livaditis; M Pehrson; K G Tillinger
Journal:  Science       Date:  1967-01-13       Impact factor: 47.728

9.  Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm.

Authors:  L Tiepolo; O Zuffardi
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

10.  Nucleotide sequence of the rightward operator of phage lambda.

Authors:  T Maniatis; A Jeffrey; D G Kleid
Journal:  Proc Natl Acad Sci U S A       Date:  1975-03       Impact factor: 11.205

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  13 in total

1.  A t(Y;15) translocation with a deletion of the proximal Yq in a boy with mixed gonadal dysgenesis.

Authors:  M Shinohara; S Minowada; Y Aso; K Yamada; Y Nakahori; T Tamura; Y Nakagome
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

Review 2.  A sterile male with 45,X0 and a Y;22 translocation.

Authors:  J Arnemann; S Schnittger; G K Hinkel; E Tolkendorf; J Schmidtke; I Hansmann
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132

3.  Molecular analysis of aberrations of Xp and Yq.

Authors:  S D Cheng; R Gasparini; U Müller
Journal:  Hum Genet       Date:  1992-02       Impact factor: 4.132

4.  Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis.

Authors:  E Margarit; A Soler; A Carrió; R Oliva; D Costa; T Vendrell; J Rosell; F Ballesta
Journal:  J Med Genet       Date:  1998-09       Impact factor: 6.318

5.  A Y/5 translocation in a 45,X male with cri du chat syndrome.

Authors:  B Weber; W Schempp; U Orth; H Seidel; A Gal
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

6.  Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male.

Authors:  M Münke; D C Page; L G Brown; B A Armson; E H Zackai; M T Mennuti; B S Emanuel
Journal:  Hum Genet       Date:  1988-11       Impact factor: 4.132

7.  Three cases of 45,X/46,XYnf mosaicism. Molecular analysis revealed heterogeneity of the nonfluorescent Y chromosome.

Authors:  D Gänshirt-Ahlert; I H Pawlowitzki; A Gal
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

8.  An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunction.

Authors:  G Annerén; M Andersson; D C Page; L G Brown; M Berg; G Läckgren; K H Gustavson; A de la Chapelle
Journal:  Am J Hum Genet       Date:  1987-10       Impact factor: 11.025

Review 9.  Molecular detection of a translocation (Y;11) (q11.2;q24) in a 45,X male with signs of Jacobsen syndrome.

Authors:  J O Van Hemel; B Eussen; E Wesby-van Swaay; B A Oostra
Journal:  Hum Genet       Date:  1992-03       Impact factor: 4.132

10.  Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11.

Authors:  M Andersson; D C Page; D Pettay; I Subrt; C Turleau; J de Grouchy; A de la Chapelle
Journal:  Hum Genet       Date:  1988-05       Impact factor: 4.132

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