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At birth and at 4 mo she had proportionate short stature, microcephaly, asymmetric micrognathia, bow\u2010shaped upper vermilion, long upper lip, submucous cleft palate, antimongoloid slant of palpebral fissures, telecanthus, prominant eyes, short neck with anterior and lateral webbing, short sternum, overlapping toes, wrist contractures, and hypertonicity. Later she was noted to have psychomotor retardation. Eleven previously published cases and our patient suggest that duplication of 6q (involving at least 6q25 \u2192 6qter) produces a highly characteristic syndrome.<\/jats:p>","DOI":"10.1002\/ajmg.1320140214","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T15:34:23Z","timestamp":1118504063000},"page":"347-351","source":"Crossref","is-referenced-by-count":14,"title":["Duplication 6q24 \u2192 6qter in an infant from a balanced paternal translocation"],"prefix":"10.1002","volume":"14","author":[{"given":"T. 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