Literature DB >> 7143390

Translocation 21q22q in an infertile human male.

A C Chandley, T B Hargreave, J M Fletcher.   

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Year:  1982        PMID: 7143390      PMCID: PMC1048923          DOI: 10.1136/jmg.19.5.366

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


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  15 in total

1.  Familial transmission of a (21q22q) translocation.

Authors:  K E Buckton; M S Newton; I J Lauder; R Mey; D Elliot; R Skinner
Journal:  Cytogenet Cell Genet       Date:  1975

2.  Down's syndrome associated with a familial (21q-; 22q+) translocation.

Authors:  M M Cohen; R G Davidson
Journal:  Cytogenetics       Date:  1967

3.  Familial mongolism due to 21/22 chromosome translocation.

Authors:  J F Jackson; W P Ashford
Journal:  JAMA       Date:  1967-05-22       Impact factor: 56.272

4.  Segregation analysis of a large t(21q22q) family.

Authors:  C J Chapman; R J Gardner; A M Veale
Journal:  J Med Genet       Date:  1973-12       Impact factor: 6.318

5.  21-22 translocation Down's syndromea family with unusual segregating patterns.

Authors:  S J Yang; H S Rosenberg
Journal:  Am J Hum Genet       Date:  1969-05       Impact factor: 11.025

6.  [Incidence of chromosome abnormalities in male sterility. Apropos of 40 cases].

Authors:  B Dutrillaux; G Le Lorier; J Salat; J Rotman
Journal:  Presse Med       Date:  1971-05-29       Impact factor: 1.228

7.  Three generations and seven family members with a t(21q22q) chromosome.

Authors:  L Zergollern
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

8.  Cytogenetics and infertility in man. II. Testicular histology and meiosis.

Authors:  A C Chandley; N Maclean; P Edmond; J Fletcher; G S Watson
Journal:  Ann Hum Genet       Date:  1976-11       Impact factor: 1.670

9.  Incidence of chromosome aberrations among 11148 newborn children.

Authors:  J Nielsen; I Sillesen
Journal:  Humangenetik       Date:  1975-10-20

10.  Quantification of human seminiferous epithelium. IV. Histological studies in 17 men with numerical and structural autosomal aberrations.

Authors:  N E Skakkebaek; M Hultén; J Philip
Journal:  Acta Pathol Microbiol Scand A       Date:  1973-03
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  3 in total

Review 1.  The genetics of human reproduction.

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

2.  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

3.  On the origin of crossover interference: A chromosome oscillatory movement (COM) model.

Authors:  Maj A Hultén
Journal:  Mol Cytogenet       Date:  2011-04-08       Impact factor: 2.009

  3 in total

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