Literature DB >> 5298975

[The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].

M L Destiné, H H Punnett, S Thovichit, A M DiGeorge, L Weiss.   

Abstract

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Year:  1967        PMID： 5298975

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


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  9 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.  Gene deletion and duplication effects on phenotype and gamma globulin levels.

Authors:  N L Rudd; P H Lamarche
Journal:  J Med Genet       Date:  1971-03       Impact factor: 6.318

6.  Partial deletion of the long arm of chromosome 18.

Authors:  A V Mikelsaar; T A Talvik
Journal:  Humangenetik       Date:  1969

7.  On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment.

Authors:  K Bender; K Burckhardt
Journal:  Humangenetik       Date:  1970

8.  A patient with a short arm deletion of chromosome 18 (46,XY,18p-).

Authors:  L Weiss; K Mayeda
Journal:  J Med Genet       Date:  1969-06       Impact factor: 6.318

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
  9 in total

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