Literature DB >> 570605

Prenatal diagnosis of a de novo Y/22 translocation.

M Verjaal, P E Treffers, Y Nagal, N J Leschot.   

Abstract

Prenatal chromosomal analysis was performed at 17 weeks' gestation because of the previous birth of a girl with trisomy 13. A seemingly balanced de novo Y/22 translocation was diagnosed. Translocations involving the Y chromosome are rare and no similar translocation, detected pre- or postnatally, could be found in published reports. The counselling problems are discussed. The pregnancy ended at term with the birth of a phenotypically normal boy. After birth, the prenatal diagnosis was confirmed and the H-Y antigen expression was determined.

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Year:  1978        PMID: 570605      PMCID: PMC1013765          DOI: 10.1136/jmg.15.6.475

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  24 in total

1.  [Translocation t(Y;14) in an azoospermic man].

Authors:  C Laurent; B Dutrillaux
Journal:  Ann Genet       Date:  1976-09

2.  [Translocation 46,X, t(Y;7)(q122;q11) in a case of male sterility].

Authors:  C Turleau; M F Croquette; J C Fourlinnie; F Desmons; J Grouchy
Journal:  Ann Genet       Date:  1976-09

3.  Testis-determining H-Y antigen in XO males of the mole-vole (Ellobius lutescens).

Authors:  Y Nagai; S Ohno
Journal:  Cell       Date:  1977-04       Impact factor: 41.582

4.  Y to X translocation in a woman with reproductive failure. A new rearrangement.

Authors:  G Khudr; K Benirschke; H L Judd; J Strauss
Journal:  JAMA       Date:  1973-10-29       Impact factor: 56.272

5.  Localization of male determining factor on short arm of Y chromosome. Case report of a baby with 46, x, t (Yp+;14q-).

Authors:  E Krmpotic; K Szego; R Modestas; G B Molabola
Journal:  Clin Genet       Date:  1972       Impact factor: 4.438

Review 6.  European experience with prenatal diagnosis of congenital disease: a survey of 6121 cases.

Authors:  H Galjaard
Journal:  Cytogenet Cell Genet       Date:  1976

7.  Translocations causing non-fluorescent Y chromosomes in human XO/XY mosaics.

Authors:  T Caspersson; M Hultén; J Jonasson; J Lindsten; A Therkelsen; L Zech
Journal:  Hereditas       Date:  1971       Impact factor: 3.271

8.  H-Y antigen and the origin of XY female wood lemmings (Myopus schisticolor).

Authors:  S S Wachtel; G C Koo; S Ohno; A Gropp; V G Dev; R Tantravahi; D A Miller; O J Miller
Journal:  Nature       Date:  1976-12-16       Impact factor: 49.962

9.  Cytogenetics and infertility in man. I. Karyotype and seminal analysis: results of a five-year survey of men attending a subfertility clinic.

Authors:  A C Chandley; P Edmond; S Christie; L Gowans; J Fletcher; A Frackiewicz; M Newton
Journal:  Ann Hum Genet       Date:  1975-10       Impact factor: 1.670

10.  Y to X translocation in man.

Authors:  H van den Berghe; P Petit; J P Fryns
Journal:  Hum Genet       Date:  1977-04-15       Impact factor: 4.132

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  2 in total

1.  Familial transmission of a translocation Y/14.

Authors:  C H Buys; G J Anders; J M Borkent-Ypma; J A Blenkers-Platter; A Y van der Hoek-van der Veen
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

Review 2.  Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome.

Authors:  R M Davis
Journal:  J Med Genet       Date:  1981-06       Impact factor: 6.318

  2 in total

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