Multiple developmental anomalies in a male infant were associated with morphological abnormalities of a No. 2 and a No. 3 chromosome. Banding studies revealed a complex rearrangement interpreted as a reciprocal translocation and an insertion following five breaks, with no apparent loss of chromosomal material. Karyotype: 46, XY, t (2p‐; 3q+), i (2q+; 3p‐) nomp (not maternally or paternally inherited).
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