Literature DB >> 5567968

An inherited pericentric chromosomal inversion (46, inv3 (p-q+)) associated with skeletal anomalies.

M M Cohen, R G Davidson.   

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Year:  1971        PMID： 5567968     DOI： 10.1016/s0022-3476(71)80156-7

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


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  3 in total

1.  Inversion homozygosity of chromosome no. 9 in a higly inbred kindred.

Authors:  D T Vine; S Yarkoni; M M Cohen
Journal:  Am J Hum Genet       Date:  1976-05       Impact factor: 11.025

2.  A fetus with recombinant of chromosome 8 inherited from her carrier father.

Authors:  A Fujimoto; J W Towner; S B Turkel; M G Wilson
Journal:  Hum Genet       Date:  1978-02-16       Impact factor: 4.132

3.  Familial pericentric inversion (3)(p12q24).

Authors:  L Lindberg; K Pelto; G H Borgström
Journal:  Hum Genet       Date:  1992-06       Impact factor: 4.132
  3 in total

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