Total: 1 |
|
PMID (PMCID) | ||
---|---|---|
1536169 |
MALE | Infant |
Trisomy 16p in a liveborn infant and review of trisomy 16p. | ||
O'Connor TA, Higgins RR. Am J Med Genet. 1992;42(3):316-9. |
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Manifestations include severe developmental delay, rounded face, sparse hair, ear anomalies, hypertelorism, cleft soft palate, a thin vermilion border of the upper lip, and left renal dysgenesis. |