A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features

  1. Quintela, I.
  2. Barros, F.
  3. Lago-Leston, R.
  4. Castro-Gago, M.
  5. Carracedo, A.
  6. Eiris, J.
Zeitschrift:
American Journal of Medical Genetics, Part A

ISSN: 1552-4833,  1552-4825

Datum der Publikation: 2015

Ausgabe: 167

Nummer: 6

Seiten: 1315-1322

Art: Artikel

DOI: 10.1002/AJMG.A.36909 GOOGLE SCHOLAR

Ziele für nachhaltige Entwicklung

Datenquelle: Scopus