Literature DB >> 5365577

Ring chromosome 18 (46, XX, 18r).

A Cenani, R A Pfeiffer, H A Simon.   

Abstract

Mesh:

Year:  1969        PMID: 5365577     DOI: 10.1007/bf00283558

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


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  9 in total

1.  IgA and ring-18 chromosome.

Authors:  B W Richards; J R Hobbs
Journal:  Lancet       Date:  1968-06-29       Impact factor: 79.321

2.  IgA and partial deletions of chromosome 18.

Authors:  J Stewart; S Go; E Ellis; A Robinson
Journal:  Lancet       Date:  1968-10-05       Impact factor: 79.321

3.  [An observation of ring chromosome 18 (18r)].

Authors:  J De Grouchy; A Herrault; J Cohen-Solal
Journal:  Ann Genet       Date:  1968-03

4.  Two patients with a 46,XX,Er chromosome constitution.

Authors:  J Leisti; U Gripenberg; E Kivalo; J Palo; B von Schoulz; E Suomalainen
Journal:  Acta Paediatr Scand       Date:  1968-09

5.  Human ring chromosome syndromes. An "E" ring associated with an abnormal phenotype.

Authors:  A K Sinha
Journal:  Acta Genet Med Gemellol (Roma)       Date:  1968-07

6.  IgA deficiency associated with partial deletion of chromosome 18.

Authors:  M Feingold; R S Schwartz; L Atkins; R Anderson; C S Bartsocas; D L Page; J W Littlefield
Journal:  Am J Dis Child       Date:  1969-02

7.  [Ring chromosome 18].

Authors:  C Hooft; P Haentjens; E Orye; P Kluyskens; G D'Hont
Journal:  Acta Paediatr Belg       Date:  1968

8.  [Deficiency of the long arm of chromosome no. 18 (46,XX,18q-)].

Authors:  A Cenani; L Schoeller; G Schubart
Journal:  Arch Kinderheilkd       Date:  1969-03

9.  A mentally retarded boy with a ring E18 chromosome.

Authors:  H Fujita; K Yamamoto; J Furuyama
Journal:  Jinrui Idengaku Zasshi       Date:  1968-10
  9 in total
  3 in total

Review 1.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

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

Review 2.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

Authors:  I W Lurie; G I Lazjuk
Journal:  Humangenetik       Date:  1972

Review 3.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23
  3 in total

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