Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1.
case_report · Level V
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- Record sourced from PubMed, PMID 7473657.
- Also identified by PMC identifier 1051640.
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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.
Medical subject headings
- Chromosome Aberrations
- Chromosome Deletion
- Chromosome Disorders
- Chromosomes, Human, Pair 1
- Developmental Disabilities
- Face