Literature DB >> 4245032

Preferential breakage of sensitive regions of human chromosomes.

B R Reeves, S D Lawler.   

Abstract

Entities:  

Mesh：

Year:  1970        PMID： 4245032     DOI： 10.1007/bf00280327

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


× No keyword cloud information.
  19 in total

1.  THE SPECIFIC EFFECTS OF STREPTONIGRIN ACTIVITY ON HUMAN CHROMOSOMES IN CULTURE.

Authors:  M M COHEN
Journal:  Cytogenetics       Date:  1963

2.  NON-RANDOM CHROMOSOMAL ABERRATIONS IN SV 40-TRANSFORMED HUMAN CELLS.

Authors:  P S Moorhead; E Saksela
Journal:  J Cell Comp Physiol       Date:  1963-08

3.  CHROMOSOMAL BREAKAGE IN A RARE AND PROBABLY GENETICALLY DETERMINED SYNDROME OF MAN.

Authors:  J GERMAN; R ARCHIBALD; D BLOOM
Journal:  Science       Date:  1965-04-23       Impact factor: 47.728

4.  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

5.  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

6.  Chromosomes and transformation of lymphocytes in lymphoproliferative disorders.

Authors:  S D Lawler; C R Pentycross; B R Reeves
Journal:  Br Med J       Date:  1968-10-26

7.  [Selective endoreduplication of the long arm of the 2 chromosome in a woman and her daughter].

Authors:  J Lejeune; B Dutrillaux; J Lafourcade; R Berger; D Abonyi; M O Rethoré
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1968-01-03

8.  [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

9.  The action of proflavin and actinomycin D in causing chromatid breakage in human cells.

Authors:  W Ostertag; W Kersten
Journal:  Exp Cell Res       Date:  1965-08       Impact factor: 3.905

10.  Chromosome damage and polyploidization induced in human peripheral leukocytes in vivo and in vitro with nitrogen mustard, 6-mercaptopurine, and A-649.

Authors:  C E Nasjleti; H H Spencer
Journal:  Cancer Res       Date:  1966-12       Impact factor: 12.701
View more
  15 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.  Studies on three rare fragile sites. 2q13, 12q13, and 17p12 segregating in one family.

Authors:  D R Romain; L M Columbano-Green; R H Smythe; R G Parfitt; O B Gebbie; C J Chapman
Journal:  Hum Genet       Date:  1986-06       Impact factor: 4.132

3.  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

4.  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

5.  Structural aberration in chromosome no.2.

Authors:  J Nielsen
Journal:  Humangenetik       Date:  1973-09-20

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

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

8.  Variations in karyotypes of normal premature babies, new-born babies and infants.

Authors:  H Müller
Journal:  Humangenetik       Date:  1971

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

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

10.  Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.

Authors:  H Hoehn; W Engel; H Reinwein
Journal:  Humangenetik       Date:  1971
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.