Literature DB >> 4132613

Antenatal genetic diagnosis in a kindred with a 15p plus chromosome.

N Hahnemann, H Eiberg.   

Abstract

Mesh：

Year:  1973        PMID： 4132613

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  4 in total

1.  Familial balanced translocation 4p+/17q- as a suggested cause of primary trisomy-21 Down's syndrome.

Authors:  K Oikawa; M Trent; R Lebovitz
Journal:  Arch Dis Child       Date:  1977-11       Impact factor: 3.791

2.  Nucleolar organizer region variants as a risk factor for Down syndrome.

Authors:  C K Jackson-Cook; D B Flannery; L A Corey; W E Nance; J A Brown
Journal:  Am J Hum Genet       Date:  1985-11       Impact factor: 11.025

Review 3.  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

4.  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
  4 in total

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