Literature DB >> 5619990

A familial variant chromosome in the 13-15 group.

P M Lord, P Cooke.   

Abstract

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Year:  1967        PMID： 5619990      PMCID： PMC1468541          DOI： 10.1136/jmg.4.2.114

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


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  2 in total

1.  THE RELATIVE LENGTH AND ARM RATIO OF THE HUMAN LATE-REPLICATING X CHROMOSOME.

Authors:  A BISHOP; M LEESE; C E BLANK
Journal:  J Med Genet       Date:  1965-06       Impact factor: 6.318

2.  Chromosome studies on randomly chosen men and women.

Authors:  W M Brown; P A Jacobs; M Brunton
Journal:  Lancet       Date:  1965-09-18       Impact factor: 79.321
  2 in total
  5 in total

1.  Cytogenetic and linkage studies of a familial 15pplus variant.

Authors:  F E Yoder; W B Bias; D S Borgaonkar; G F Bahr; I I Yoder; O C Yoder; H M Golomb
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

2.  A further example of familial Gp+ associated with trisomy G.

Authors:  I Subrt
Journal:  Humangenetik       Date:  1970

3.  A family with an inherited marker chromosome (46,D-,mar15+).

Authors:  R M Bannerman; M J Marinello; M M Cohen; C Lockwood
Journal:  Am J Hum Genet       Date:  1971-05       Impact factor: 11.025

4.  Inherited pericentric inversion of a group D (13-15) chromosome.

Authors:  R B Surana; P E Conen
Journal:  J Med Genet       Date:  1972-03       Impact factor: 6.318

5.  Cytogenetic studies on mid-trimester abortuses.

Authors:  P Ruzicska; A Czeizel
Journal:  Humangenetik       Date:  1970
  5 in total

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