Answer to Letter to the Editor regarding the article "Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletion"

Eur J Med Genet. 2020 Oct;63(10):103993. doi: 10.1016/j.ejmg.2020.103993. Epub 2020 Jun 20.

Authors

Giulia Pascolini¹, Michele Valiante², Irene Bottillo², Luigi Laino², Nicole Fleischer³, Alessandro Ferraris², Paola Grammatico²

Affiliations

¹ Medical Genetics, Department of Molecular Medicine, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy. Electronic address: giulia.pascolini@uniroma1.it.
² Medical Genetics, Department of Molecular Medicine, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy.
³ FDNA Inc., Boston, MA, USA.

PMID: 32574611
DOI: 10.1016/j.ejmg.2020.103993

No abstract available

Publication types

Letter
Comment

MeSH terms

DNA-Binding Proteins
Hand Deformities, Congenital*
Humans
Intellectual Disability* / genetics
Micrognathism* / genetics
Neck
Syndrome
Transcription Factors / genetics
Twins, Monozygotic / genetics

Substances

ARID1B protein, human
DNA-Binding Proteins
Transcription Factors