Abstract
A patient is described with multiple congenital anomalies and probable tetrasomy 18p resulting from an extra i(18p) in an otherwise normal karyotype. Review of ten previously reported i(18p) cases allowed the tentative characterisation of a tetrasomy 18p syndrome.
Original language | English (US) |
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Pages (from-to) | 144-147 |
Number of pages | 4 |
Journal | Journal of medical genetics |
Volume | 20 |
Issue number | 2 |
DOIs | |
State | Published - 1983 |
Externally published | Yes |
ASJC Scopus subject areas
- Genetics
- Genetics(clinical)