Literature DB >> 5295700

[Partial deletion of the long arm of chromosome 18. Individualization of a new morbid state].

J Lejeune, R Berger, J Lafourcade, M O Réthoré.   

Abstract

Mesh：

Year:  1966        PMID： 5295700

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  19 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.  Deletion of the long arms of chromosome 18 (46,XX,18q-) associated with absence of IgA and hypothyroidism in an adult.

Authors:  M J Faed; R Whyte; C R Paterson; M McCathie; J Robertson
Journal:  J Med Genet       Date:  1972-03       Impact factor: 6.318

6.  [Ocular manifestations in diseases caused by aberrations in non-sexual chromosomes].

Authors:  H Saraux
Journal:  J Med Genet       Date:  1970-09       Impact factor: 6.318

7.  Letter: Acromial dimples: a benign familial trait.

Authors:  J W Bianchine
Journal:  Am J Hum Genet       Date:  1974-05       Impact factor: 11.025

Review 8.  [On the problem of assigning genes to definite human autosomes with the aid of chromosome aberrations].

Authors:  K Bender; H Ritter; U Wolf
Journal:  Humangenetik       Date:  1967

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

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

10.  The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2.

Authors:  G A Silverman; S S Schneider; H F Massa; A Flint; M Lalande; J C Leonard; J Overhauser; G van den Engh; B J Trask
Journal:  Am J Hum Genet       Date:  1995-04       Impact factor: 11.025
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