Literature DB >> 4238957

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

W Schmid, D Vischer.   

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Year:  1969        PMID： 4238957     DOI： 10.1007/bf00278689

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


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  7 in total

1.  THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES.

Authors:  M A FERGUSON-SMITH
Journal:  Cytogenetics       Date:  1964

2.  The sites and relative frequencies of secondary constrictions in human somatic chromosomes.

Authors:  M A FERGUSON-SMITH; M E FERGUSON-SMITH; P M ELLIS; M DICKSON
Journal:  Cytogenetics       Date:  1962

3.  Enhancement of secondary constrictions and the heterochromatic X in human cells.

Authors:  E SAKSELA; P S MOORHEAD
Journal:  Cytogenetics       Date:  1962

4.  Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors:  P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal:  Exp Cell Res       Date:  1960-09       Impact factor: 3.905

5.  Partial-trisomy syndromes. II. An insertion as cause of the OFD syndrome in mother and daughter.

Authors:  K PATAU; E THERMAN; S L INHORN; D W SMITH; A L RUESS
Journal:  Chromosoma       Date:  1961       Impact factor: 4.316

6.  [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

7.  EFFECTS OF MITOMYCIN C ON HUMAN CHROMOSOMES.

Authors:  M M COHEN; M W SHAW
Journal:  J Cell Biol       Date:  1964-11       Impact factor: 10.539
  7 in total
  18 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

2.  The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(gh',RHG,CAG,CBG).

Authors:  E Donti; G Venti; V Bocchini; G Rosi; R Armellini; N Trabalza
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

3.  Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1979-03       Impact factor: 11.025

4.  The correspondence between quinacrine banding patterns and sites of secondary constrictions in human chromosomes.

Authors:  I H Pawlowitzki
Journal:  Humangenetik       Date:  1972

5.  Preferential breakage of sensitive regions of human chromosomes.

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

6.  [Partial tetrasomy of number 9 chromosome, and mosaicism in a child with multiple malformations (author's transl)].

Authors:  D Ghymers; B Hermann; C Distèche; J Frederic
Journal:  Humangenetik       Date:  1973-12-10

7.  [Partial trisomy for the short arm of chromosome 4 with translocation 4p-,18q+ in the father].

Authors:  A Schinzel; W Schmid
Journal:  Humangenetik       Date:  1972

8.  A familial variant of chromosome 9.

Authors:  C G Palmer; J Schroder
Journal:  J Med Genet       Date:  1971-06       Impact factor: 6.318

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

Authors:  G Schwanitz; H D Rott; M W Köllermann
Journal:  Humangenetik       Date:  1971

10.  Cytological and cytogenetical studies on brain tumors. II. Hyperdiploidy, a rare event in human primary meningiomas.

Authors:  H Zankl; H Singer; K D Zang
Journal:  Humangenetik       Date:  1971
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