Literature DB >> 7069747

Cytogenetic and histological studies of testicular biopsies from subfertile men with chromosome anomaly.

M J Faed, M A Lamont, K Baxby.   

Abstract

Testicular biopsies from eight men with abnormal karyotypes have been examined for histological and cytogenetic evidence of disturbances of meiosis. Quantitative analysis of this material showed one, with a 13;14 Robertsonian translocation, to have apparently normal spermatogenesis. Three patients, one with a 47,XYY and two with 45,XY, inv 9 karyotypes, had an overall depression of spermatogenesis. Four others, all with major chromosomal abnormalities, had apparently normal spermatogenesis until the primary spermatocyte stage. Two of these had sex autosomal translocations. One, 45,Y,t(X;21), had a complete block at MI, the other, 46,X,t(Y;16), had a partial block at spermatid formation. One man with a reciprocal 2;10 translocation showed delay at all stages beyond spermatocyte formation and one man with an inversion of chromosome 3 showed impaired spermatid maturation.

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Year:  1982        PMID: 7069747      PMCID: PMC1048819          DOI: 10.1136/jmg.19.1.49

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


  24 in total

1.  [Mitotic and meiotic analysis of an Y-autosome translocation(author's transl)].

Authors:  B Dutrillaux; J Gueguen
Journal:  Humangenetik       Date:  1975

2.  Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the "cri du chat" syndrome.

Authors:  M J Faed; V J Marrian; J Robertson; E B Robson; P J Cook
Journal:  Cytogenetics       Date:  1972

3.  Failure of transmission of the extra chromosome in subjects with 47,XYY karyotype.

Authors:  J Melnyk; H Thompson; A J Rucci; F Vanasek; S Hayes
Journal:  Lancet       Date:  1969-10-11       Impact factor: 79.321

4.  Translocation heterozygosity and associated subfertility in man.

Authors:  A C Chandley; S Christie; J Fletcher; A Frackiewicz; P A Jacobs
Journal:  Cytogenetics       Date:  1972

5.  An inherited X-autosome translocation in man.

Authors:  K E Buckton; P A Jacobs; L A Rae; M S Newton; R Sanger
Journal:  Ann Hum Genet       Date:  1971-10       Impact factor: 1.670

6.  Testicular biopsy score count--a method for registration of spermatogenesis in human testes: normal values and results in 335 hypogonadal males.

Authors:  S G Johnsen
Journal:  Hormones       Date:  1970

7.  [Sterility and familial t (1q-;Xq+) translocation].

Authors:  B Dutrillaux; J Couturier; J Rotman; J Salat; J Lejeune
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1972-06-12

Review 8.  The role of X-chromosome inactivation during spermatogenesis (Drosophila-allocycly-chromosome evolution-male sterility-dosage compensation).

Authors:  E Lifschytz; D L Lindsley
Journal:  Proc Natl Acad Sci U S A       Date:  1972-01       Impact factor: 11.205

9.  Nature and consequences of induced chromosome damage in mammals.

Authors:  A G Searle
Journal:  Genetics       Date:  1974-09       Impact factor: 4.562

10.  Quantification of human seminiferous epithelium. II. Histological studies in eight 47,XYY men.

Authors:  N E Skakkebaek; M Hultén; P Jacobsen; M Mikkelsen
Journal:  J Reprod Fertil       Date:  1973-03
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  16 in total

1.  Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion.

Authors:  V Shashi; W L Golden; P S Allinson; S H Blanton; C von Kap-Herr; T E Kelly
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

2.  Partial trisomy 13q resulting from a paternal reciprocal Yq;13q translocation.

Authors:  J Nikolis; K Ivanović; V Diklić
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

Review 3.  The genetics of human reproduction.

Authors:  A C Chandley
Journal:  Experientia       Date:  1986-10-15

4.  Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.

Authors:  S E Bodrug; J R Roberson; L Weiss; P N Ray; R G Worton; D L Van Dyke
Journal:  J Med Genet       Date:  1990-07       Impact factor: 6.318

5.  Familial inv(1) (p3500q21.3) associated with azoospermia.

Authors:  H Rivera; M C Alvarez-Arratia; M Moller; M Díaz; J M Cantú
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  Meiotic studies in a series of 1100 infertile and sterile males.

Authors:  J Egozcue; C Templado; F Vidal; J Navarro; F Morer-Fargas; S Marina
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

7.  Studies on chiasma frequency and distribution in two fertile men carrying reciprocal translocations; one with a t(9;10) karyotype and one with a t(Y;10) karyotype.

Authors:  D A Laurie; R W Palmer; M A Hultén
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  Meiotic studies and synaptonemal complex analysis in two infertile males with a 13/14 balanced translocation.

Authors:  C Templado; F Vidal; J Navarro; S Marina; J Egozcue
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Hypospadias and gynecomastia in a male associated with autosomal balanced translocation.

Authors:  D S Krishna Murthy; V C Shah; A K Chadha; S K Murthy; A B Desai
Journal:  Indian J Pediatr       Date:  1985 Jul-Aug       Impact factor: 1.967

10.  Molecular and cytogenetic characterization of two azoospermic patients with X-autosome translocation.

Authors:  Suman Lee; Sook-Hwan Lee; Tae-Gyu Chung; Hyun-Joo Kim; Tae-Ki Yoon; In-Pyung Kwak; Sang-Hee Park; Won-Tae Cha; Sung-Won Cho; Kwang-Yul Cha
Journal:  J Assist Reprod Genet       Date:  2003-09       Impact factor: 3.412

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