Literature DB >> 5101665

[Enlarged secondary constriction of chromosome C9 in mother and child].

G Schwanitz, H D Rott, M W Köllermann.   

Abstract

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Year:  1971        PMID： 5101665     DOI： 10.1007/bf00274747

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  6 in total

1.  Spontaneous fragility of an abnormally wide secondary constriction region in a human chromosome no. 9.

Authors:  W Schmid; D Vischer
Journal:  Humangenetik       Date:  1969

2.  Preferential breakage of sensitive regions of human chromosomes.

Authors:  B R Reeves; S D Lawler
Journal:  Humangenetik       Date:  1970

3.  [Two observations of identical breakages in the same group C chromosome].

Authors:  I Emerit; J De Grouchy; P Vernant
Journal:  Ann Genet       Date:  1968-03

4.  A cytogenetic study of familial deafness.

Authors:  H Dar; S T Winter
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

5.  [A specific aberration of a C group chromosome in several members of a family].

Authors:  E Kunze-Mühl; P Fischer; E Golob
Journal:  Humangenetik       Date:  1970

6.  [A case of structural aberration of the chromosome A2].

Authors:  E Golob; E Kunze-Mühl; F Friedrich
Journal:  Humangenetik       Date:  1970-09-17
  6 in total
  1 in total

1.  A case of trisomy for the short arm of chromosome no. 9(+9(p)).

Authors:  M E Käosaar; A V Mikelsaar; T A Talvik; R V Mikelsaar
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132
  1 in total

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