Literature DB >> 5295699

[Deletion of the short arm of chromosome 18].

J de Grouchy, J Bonnette, C Salmon.   

Abstract

Mesh：

Year:  1966        PMID： 5295699

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


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  8 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.  [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

4.  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

5.  Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum.

Authors:  P Fischer; E Golob; F Friedrich; E Kunze-Mühl; W Doleschel; H Aichmair
Journal:  J Med Genet       Date:  1970-03       Impact factor: 6.318

6.  Deletion of short arm of a chromosome 18 (46, XX, 18 p-).

Authors:  H Reinwein; H Ritter; U Wolf
Journal:  Humangenetik       Date:  1967-11-29

7.  18p-Mosaicism: case report and review.

Authors:  T Motegi; A Ichikawa; M Noda; G Hashimoto; M Kaga
Journal:  Hum Genet       Date:  1978-10-31       Impact factor: 4.132

8.  The 18 p-syndrome. Report of four cases.

Authors:  J Faust; M Habedank; C Nieuwenhuijsen
Journal:  Eur J Pediatr       Date:  1976-08-16       Impact factor: 3.183
  8 in total

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