Literature DB >> 5764448

Structural polymorphism in chromosome 17.

E Schmid, M Bauchinger.   

Abstract

Mesh:

Year:  1969        PMID: 5764448     DOI: 10.1038/221387a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


× No keyword cloud information.
  9 in total

1.  The fragile site (17)(p12): induction by AT-specific DNA-ligands and population cytogenetics.

Authors:  M Schmid; W Feichtinger; C Deubelbeiss; E Weller
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

2.  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

Review 3.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

Authors:  J Kunze; E Stephan; M Tolksdorf
Journal:  Humangenetik       Date:  1972

4.  Non-condensation of one segment of a chromosome No. 2 in a male with an otherwise normal karyotype (and severe hypospadias).

Authors:  E M Bühler; U Luchsinger; U K Bühler; K Méhes; G R Stalder
Journal:  Humangenetik       Date:  1970

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

Authors:  J H Priest; D C Peakman; S R Patil; A Robinson
Journal:  J Med Genet       Date:  1970-06       Impact factor: 6.318

6.  Constitutional chromosomal breakage.

Authors:  F Giraud; S Ayme; J F Mattei; M G Mattei
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

7.  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

8.  Functional implications of differential chromosome banding.

Authors:  H Hoehn
Journal:  Am J Hum Genet       Date:  1975-09       Impact factor: 11.025

9.  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

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.