De-novo interstitial 2.33 Mb deletion in 8q24.3: new insights on a very rare partial monosomy syndrome

Clin Dysmorphol. 2018 Jul;27(3):97-100. doi: 10.1097/MCD.0000000000000224.

Susan Akbaroghli^{1

2}, Seyed H Tonekaboni^{3

2}, Roxana Kariminejad⁴, Thomas Liehr⁵, Emanuele G Coci^{6

7}

¹ Department of Pediatrics, Clinical Genetics Division.
² Pediatric Neurology Research Center, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences.
³ Child Neurology Department.
⁴ Kariminejad-Najmabadi Pathology and Genetics Center, Tehran, Iran.
⁵ Institute of Human Genetics, Jena University Hospital, Jena.
⁶ Department of Pediatric Neurology, Clinic for Pediatrics, Braunschweig.
⁷ Department of Neuropediatrics, University Children's Hospital, Ruhr-University Bochum, Bochum, Germany.

No abstract available

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