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. 1995 Aug;32(8):636–637. doi: 10.1136/jmg.32.8.636

Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1.

J S Barton 1, J O'Loughlin 1, R T Howell 1, R L'e Orme 1
PMCID: PMC1051640  PMID: 7473657

Abstract

We report an 18 month old girl with developmental delay, dysmorphic features, and a karyotype 46,XX,del (1) (p32.1p32.3). To our knowledge the clinical features associated with this deletion have not been reported previously.

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Selected References

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

  1. Howard P. J., Porteus M. Deletion of chromosome 1p: a short review. Clin Genet. 1990 Feb;37(2):127–131. doi: 10.1111/j.1399-0004.1990.tb03489.x. [DOI] [PubMed] [Google Scholar]
  2. Lai M. M., Robards M. F., Berry A. C., Fear C. N., Hart C. Two cases of interstitial deletion 1p. J Med Genet. 1991 Feb;28(2):128–130. doi: 10.1136/jmg.28.2.128. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Yoshino M., Watanabe Y., Harada N., Abe K. De novo interstitial deletion of 1p (pter----p34.1::p32.3----qter). J Med Genet. 1991 Aug;28(8):539–540. doi: 10.1136/jmg.28.8.539. [DOI] [PMC free article] [PubMed] [Google Scholar]

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