Search Results - "Mak, Bryan C."
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Craniofacial features of 3q29 deletion syndrome: Application of next‐generation phenotyping technology
Published in American journal of medical genetics. Part A (01-07-2021)“…3q29 deletion syndrome (3q29del) is a recurrent deletion syndrome associated with neuropsychiatric disorders and congenital anomalies. Dysmorphic facial…”
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