Literature DB >> 5800650

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

A Cenani, L Schoeller, G Schubart.   

Abstract

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Year:  1969        PMID： 5800650

Source DB:  PubMed          Journal:  Arch Kinderheilkd        ISSN： 0003-9179


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  7 in total

1.  The cytogenetics of 90 patients with idiopathic mental retardation/malformation syndromes and of 90 normal subjects.

Authors:  C T Doyle
Journal:  Hum Genet       Date:  1976-07-27       Impact factor: 4.132

Review 2.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

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

Review 3.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

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

Review 4.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

5.  Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation.

Authors:  T H Thelen; D J Abrams; R O Fisch
Journal:  Am J Hum Genet       Date:  1971-07       Impact factor: 11.025

6.  Ring chromosome 18 (46, XX, 18r).

Authors:  A Cenani; R A Pfeiffer; H A Simon
Journal:  Humangenetik       Date:  1969

7.  Structural aberrations of chromosome 18. II. The 18q- syndrome. Report of three cases.

Authors:  A Schinzel; K Hayashi; W Schmid
Journal:  Humangenetik       Date:  1975
  7 in total

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