Literature DB >> 5519600

Significance of chromosome 17ps+ in three generations of a family.

J H Priest, D C Peakman, S R Patil, A Robinson.   

Abstract

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Year:  1970        PMID： 5519600      PMCID： PMC1468801          DOI： 10.1136/jmg.7.2.142

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


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  12 in total

1.  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

2.  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

3.  THE SOMATIC CHROMOSOMAL CONSTITUTION OF SOME HUMAN SUBJECTS WITH GENETIC DEFECTS.

Authors:  J H Tjio; T T Puck; A Robinson
Journal:  Proc Natl Acad Sci U S A       Date:  1959-07       Impact factor: 11.205

4.  Chromosomal abnormalities and congenital heart disease.

Authors:  I Emerit; J de Grouchy; P Vernant; P Corone
Journal:  Circulation       Date:  1967-12       Impact factor: 29.690

5.  A homozygous chromosomal variant.

Authors:  J M Berg; J A Faunch; M J Pendrey; L S Penrose; M A Ridler; A Shapiro
Journal:  Lancet       Date:  1969-03-08       Impact factor: 79.321

6.  Structural polymorphism in chromosome 17.

Authors:  E Schmid; M Bauchinger
Journal:  Nature       Date:  1969-01-25       Impact factor: 49.962

7.  Probable assignment of the Duffy blood group locus to chromosome 1 in man.

Authors:  R P Donahue; W B Bias; J H Renwick; V A McKusick
Journal:  Proc Natl Acad Sci U S A       Date:  1968-11       Impact factor: 11.205

8.  Heritable morphological difference between the two chromosomes no. 16 in humans.

Authors:  A J Therkelsen; L U Lamm
Journal:  Hereditas       Date:  1967       Impact factor: 3.271

Review 9.  The cri-du-chat syndrome with an apparently normal karyotype.

Authors:  D D McGavin; J S Cant; M A Ferguson-Smith; P M Ellis
Journal:  Lancet       Date:  1967-08-12       Impact factor: 79.321

10.  Familial congenital heart disease. II. Chromosomal studies.

Authors:  J German; K H Ehlers; M A Engle
Journal:  Circulation       Date:  1966-09       Impact factor: 29.690
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  4 in total

1.  Cytochemical analysis on a case of familial 17ps.

Authors:  W Au; J A Witek
Journal:  Hum Genet       Date:  1979-04-27       Impact factor: 4.132

2.  Chromosome 17 has a real fragile site at p12.

Authors:  F Shabtai; D Klar; I Halbrecht
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

3.  Silver staining studies on the short arm variant of human chromosome 17.

Authors:  N Oliver; U Francke; K M Taylor
Journal:  Hum Genet       Date:  1978-05-16       Impact factor: 4.132

4.  Parental trisomy 21 mosaicism.

Authors:  D J Harris; M L Begleiter; J Chamberlin; L Hankins; R E Magenis
Journal:  Am J Hum Genet       Date:  1982-01       Impact factor: 11.025
  4 in total

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