NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families.
Saved in:
| Title: | NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families. |
|---|---|
| Authors: | Al Shehhi M; Department of Clinical Genetics, OLCHC, Dublin12, Ireland., Forman EB; Children's University Hospital, Temple St., Dublin, Ireland. Electronic address: eva.forman@cuh.ie., Fitzgerald JE; Trinity Centre for Health Sciences, St. James's Hospital, Dublin, Ireland; Trinity Institute of Neuroscience, Dublin, Ireland., McInerney V; HRB Clinical Research Facility, National University of Ireland Galway, Newcastle Road Galway, Ireland., Krawczyk J; HRB Clinical Research Facility, National University of Ireland Galway, Newcastle Road Galway, Ireland., Shen S; Regenerative Medicine Institute, School of Medicine, (NUI) Galway, Ireland., Betts DR; Department of Clinical Genetics, OLCHC, Dublin12, Ireland., Ardle LM; Department of Clinical Genetics, OLCHC, Dublin12, Ireland., Gorman KM; Children's University Hospital, Temple St., Dublin, Ireland., King MD; Children's University Hospital, Temple St., Dublin, Ireland; Academic Center on Rare Diseases, School of Medicine and Medical Science, University College Dublin, Ireland., Green A; Department of Clinical Genetics, OLCHC, Dublin12, Ireland; Children's University Hospital, Temple St., Dublin, Ireland; Academic Center on Rare Diseases, School of Medicine and Medical Science, University College Dublin, Ireland., Gallagher L; Trinity Centre for Health Sciences, St. James's Hospital, Dublin, Ireland., Lynch SA; Department of Clinical Genetics, OLCHC, Dublin12, Ireland; Children's University Hospital, Temple St., Dublin, Ireland; Academic Center on Rare Diseases, School of Medicine and Medical Science, University College Dublin, Ireland. |
| Source: | European journal of medical genetics [Eur J Med Genet] 2019 Mar; Vol. 62 (3), pp. 204-209. Date of Electronic Publication: 2018 Jul 18. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
Be the first to leave a comment!
