Literature DB >> 3573006

De novo inv(5)(p15q22), del(5)(p15) in a boy with cri du chat syndrome.

H Rivera, R Velázquez, L García-Esquivel, R Martínez Martínez, J M Cantú.   

Abstract

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Year:  1987        PMID： 3573006      PMCID： PMC1049958          DOI： 10.1136/jmg.24.3.186

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  3 in total

1.  Molecular approach to analyzing the human 5p deletion syndrome, cri du chat.

Authors:  L R Carlock; J J Wasmuth
Journal:  Somat Cell Mol Genet       Date:  1985-05

Review 2.  Pericentric inversions. Problems and significance for clinical genetics.

Authors:  P Kaiser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

Review 3.  The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features.

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

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