Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1987 Mar;24(3):186. doi: 10.1136/jmg.24.3.186

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
PMCID: PMC1049958  PMID: 3573006

Full text

PDF

Page 186

186

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Carlock L. R., Wasmuth J. J. Molecular approach to analyzing the human 5p deletion syndrome, cri du chat. Somat Cell Mol Genet. 1985 May;11(3):267–276. doi: 10.1007/BF01534683. [DOI] [PubMed] [Google Scholar]
  2. Kaiser P. Pericentric inversions. Problems and significance for clinical genetics. Hum Genet. 1984;68(1):1–47. doi: 10.1007/BF00293869. [DOI] [PubMed] [Google Scholar]
  3. Niebuhr E. The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features. Hum Genet. 1978 Nov 16;44(3):227–275. doi: 10.1007/BF00394291. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES