Child with Deletion 9p Syndrome Presenting with Craniofacial Dysmorphism, Developmental Delay, and Multiple Congenital Malformations

Ítems similars

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• Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1.
  per: Barton, J S, et al.
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• Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay
  per: Seo, Go Hun, et al.
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