Work

A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAX

Year: 2014

Type: article

Study design: Observational Study

Source: European Journal of Medical Genetics

DOI: 10.1016/j.ejmg.2014.08.007

Authors: Morad Ansari, Jacqueline K. Rainger, Jennie E. Murray, Isabel Hanson, Helen V. Firth, Felicity Mehendale, Jeanne Amiel, Christopher T. Gordon, Antonio Percesepe, Laura Mazzanti, Alan Fryer, Paola Ferrari, Koenraad Devriendt, I. Karen Temple, David R. FitzPatrick

Institutions: Institute of Genetics and Cancer, MRC Human Genetics Unit, University of Edinburgh, Western General Hospital, Wellcome Sanger Institute, Royal Hospital for Sick Children, Hôpital Necker-Enfants Malades, Inserm, Sorbonne Paris Cité, Institut des Maladies Génétiques Imagine, Université Paris Descartes, University of Modena and Reggio Emilia, University of Bologna, Alder Hey Children's Hospital, KU Leuven, Princess Anne Hospital, University of Southampton

Language: English

Topic: Cleft Lip and Palate Research

Subfield: Oral Surgery

Field: Dentistry

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: green

Funders: Wellcome Trust, Medical Research Council

OpenAlex ID: W2110052830

FWCI: 3.702

Cites: 25

Cited by: 26

Related to: 10