Literature DB >> 5848077

"Cri du chat" syndrome. Partial deletion of the short arm of a chromosome No. 5. Report of a case.

T W Hustinx, J C Wijffels.   

Abstract

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Year:  1965        PMID： 5848077

Source DB:  PubMed          Journal:  Maandschr Kindergeneeskd        ISSN： 0024-869X


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  4 in total

Review 1.  [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

2.  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

3.  Duplication deficiency syndrome in familial translocation (2q-;5p+).

Authors:  J B Bijlsma; H de France; E M Bleeker-Wagemakers
Journal:  Humangenetik       Date:  1971

Review 4.  The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features.

Authors:  E Niebuhr
Journal:  Hum Genet       Date:  1978-11-16       Impact factor: 4.132
  4 in total

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