Abstract
We report an 18 month old girl with developmental delay, dysmorphic features, and a karyotype 46, XX, del (1) (p32. lp32.3). To our knowledge the clinical features associated with this deletion have not been reported previously.
Cite
CITATION STYLE
APA
Barton, J. S., Loughlin, J. O., Howell, R. T., & Orme, R. L. E. (1995). Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1. Journal of Medical Genetics, 32(8), 636–637. https://doi.org/10.1136/jmg.32.8.636
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