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Phenotypic variability of the 1q21.1 microdeletion syndrome in members of the same family: relevance of detection of neuropsychiatric disorders for diagnosis of genetic syndromes

作者：Natera De Benito Daniel; Vidal Esteban Arantxa; Sanchez Del Pozo Jaime; Moreno Garcia Marta; Suela Rubio Javier; Cruz Rojo Jaime; Jose Rivero Martin Maria
来源：Revista de Neurologia, 2015, 61(12): 550-556.
  • 出版日期2015-12-16
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更新时间：2018-04-09 13:45