Literature DB >> 4349228

A Y-autosome translocation 46,X,t(Yq-7q+) associated with multiple congenital anomalies.

A J Develing, F A Conte, C J Epstein.   

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Year:  1973        PMID: 4349228     DOI: 10.1016/s0022-3476(73)80132-5

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


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  11 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.  X/XYq - mosaicism and mixed gonadal dysgenesis.

Authors:  E Yunis; R Silva; E Ramirez; M A Nossa
Journal:  J Med Genet       Date:  1977-08       Impact factor: 6.318

3.  Three cases of sex chromosome mosaicism with a nonfluorescent Y.

Authors:  K Madan; L Gooren; J Schoemaker
Journal:  Hum Genet       Date:  1979-02-15       Impact factor: 4.132

4.  Robertsonian translocation between the chromosome Y and 15.

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

Review 5.  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

6.  An azoospermic male with a Y/autosome translocation.

Authors:  I Lopez Pajares; A Delicado; P V Cobos; F Sanchez Corral; C Cuadrado
Journal:  Hum Genet       Date:  1979-01-25       Impact factor: 4.132

7.  Mitotic and meiotic analysis of a reciprocal translocation t(Y;3) in an azoospermic male.

Authors:  J Gonzales; S Lesourd; B Dutrillaux
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

8.  Paracentric inversion of a human chromosome 7.

Authors:  H Shimba; K Ohtaki; K Tanabe; T Sofuni
Journal:  Hum Genet       Date:  1976-01-28       Impact factor: 4.132

9.  Prenatal diagnosis of a de novo Y/22 translocation.

Authors:  M Verjaal; P E Treffers; Y Nagal; N J Leschot
Journal:  J Med Genet       Date:  1978-12       Impact factor: 6.318

10.  Mosaicism presumably related to a Y/6 translocation in a boy with multiple congenital abnormalities.

Authors:  L Wisniewski; J V Higgins
Journal:  J Med Genet       Date:  1977-10       Impact factor: 6.318

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