Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1992 Feb;29(2):141. doi: 10.1136/jmg.29.2.141-b

Maxillonasal dysplasia (Binder's syndrome) and chondrodysplasia punctata.

F Serville
PMCID: PMC1015873  PMID: 1613767

Full text

PDF

Page 141

141

Selected References

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

  1. Petit C., Melki J., Levilliers J., Serville F., Weissenbach J., Maroteaux P. An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature. Hum Genet. 1990 Jul;85(2):247–250. doi: 10.1007/BF00193206. [DOI] [PubMed] [Google Scholar]
  2. Sheffield L. J., Halliday J. L., Jensen F. Maxillonasal dysplasia (Binder's syndrome) and chondrodysplasia punctata. J Med Genet. 1991 Jul;28(7):503–504. doi: 10.1136/jmg.28.7.503. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES