Literature DB >> 13881132

Enlarged satellites as a familial chromosome marker.

H L COOPER, K HIRSCHHORN.   

Abstract

Keywords:  CHROMOSOMES

Mesh:

Substances:

Year:  1962        PMID: 13881132      PMCID: PMC1932273     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


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  13 in total

1.  Enlarged satellites and multiple malformations in the same pedigree.

Authors:  J R ELLIS; L S PENROSE
Journal:  Ann Hum Genet       Date:  1961-10       Impact factor: 1.670

2.  Culture of human white cells using differential leucocyte separation.

Authors:  J HASTINGS; S FREEDMAN; O RENDON; H L COOPER; K HIRSCHHORN
Journal:  Nature       Date:  1961-12-23       Impact factor: 49.962

3.  Human chromosome complements in normal somatic cells in culture.

Authors:  E H CHU; N H GILES
Journal:  Am J Hum Genet       Date:  1959-03       Impact factor: 11.025

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.  Recent developments in human cytogenetics.

Authors:  O J MILLER; H L COOPER; K HIRSCHHORN
Journal:  Eugen Q       Date:  1961-03

6.  Human cytogenetics: its present place and future possibilities.

Authors:  C E FORD
Journal:  Am J Hum Genet       Date:  1960-03       Impact factor: 11.025

7.  THE SOMATIC CHOMOSOMES OF MAN.

Authors:  J H Tjio; T T Puck
Journal:  Proc Natl Acad Sci U S A       Date:  1958-12-15       Impact factor: 11.205

8.  Gm Phenotypes and Genotypes in U. S. Whites and Negroes; in American Indians and Eskimos; in Africans; and in Micronesians.

Authors:  A G Steinberg; R Stauffer; B S Blumberg; H Fudenberg
Journal:  Am J Hum Genet       Date:  1961-06       Impact factor: 11.025

9.  THE HUMAN CHROMOSOMAL SATELLITES IN NORMAL PERSONS AND IN TWO PATIENTS WITH MARFAN'S SYNDROME.

Authors:  J H Tjio; T T Puck; A Robinson
Journal:  Proc Natl Acad Sci U S A       Date:  1960-04       Impact factor: 11.205

10.  Genetics of somatic mammalian cells. II. Chromosomal constitution of cells in tissue culture.

Authors:  J H TJIO; T T PUCK
Journal:  J Exp Med       Date:  1958-08-01       Impact factor: 14.307

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  17 in total

1.  The satellited chromosomes of man with reference to the marfan syndrome.

Authors:  S D HANDMAKER
Journal:  Am J Hum Genet       Date:  1963-03       Impact factor: 11.025

2.  A 13-15/21 translocation chromosome in carrier father and mongol son.

Authors:  F R SERGOVICH; H C SOLTAN; D H CARR
Journal:  Can Med Assoc J       Date:  1962-10-20       Impact factor: 8.262

3.  Abnormal chromosome 22 and recurrence of trisomy-22 syndrome.

Authors:  B S Emanuel; E H Zackai; M M Aronson; W J Mellman; P S Moorhead
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

4.  Pitfalls in the use of chromosome variants for paternity dispute cases.

Authors:  Y Nakagome; T Kitagawa; K Iinuma; E Matsunaga; T Shinoda
Journal:  Hum Genet       Date:  1977-07-26       Impact factor: 4.132

5.  Atypical acrocentric chromosomes in Negro and Caucasian Mongols.

Authors:  M N Starkman; M W Shaw
Journal:  Am J Hum Genet       Date:  1967-03       Impact factor: 11.025

6.  Short arm enlargement in acrocentric chromosomes.

Authors:  V E Sands
Journal:  Am J Hum Genet       Date:  1969-05       Impact factor: 11.025

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

Authors:  I Subrt
Journal:  Humangenetik       Date:  1970

8.  Frequency of satellite association in individuals with structural abnormalities of nucleolus organiser region.

Authors:  A De Capoa; A Rocchi; F Gigliani
Journal:  Humangenetik       Date:  1973-04-16

9.  [Chromosome studies in couples with repeated abortions].

Authors:  H D Rott; E Richter; W D Rummel; G Schwanitz
Journal:  Arch Gynakol       Date:  1972

10.  A marker chromosome number 14 with double satellite obseved in two generations: an unbalanced chromosome constitution associated with normal phenotype.

Authors:  F Gigliani; A De Capoa; A Rocchi
Journal:  Humangenetik       Date:  1972
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