Literature DB >> 5308384

[18p- syndrome. A further case].

N Ayraud, G Darcourt, M D'Oelsnitz, J Poujol, J Lavagna, C Capdeville.   

Abstract

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Year:  1969        PMID： 5308384

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


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  7 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

Review 4.  Population cytogenetics, assignment of gene loci in autosomes, karyotype-phenotype correlations. A progress report on human cytogenetics.

Authors:  E Passarge
Journal:  Humangenetik       Date:  1970

5.  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

6.  Dicentric chromosome due to an unusual fusion.

Authors:  I Subrt; B Blehová; O Táborský
Journal:  Humangenetik       Date:  1971

Review 7.  Chromosomal aberrations and schizophrenia. Autosomes.

Authors:  A S Bassett
Journal:  Br J Psychiatry       Date:  1992-09       Impact factor: 9.319
  7 in total

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