NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome. Issue 12 (9th December 2004)
- Record Type:
- Journal Article
- Title:
- NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome. Issue 12 (9th December 2004)
- Main Title:
- NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome
- Authors:
- Borck, G
Redon, R
Sanlaville, D
Rio, M
Prieur, M
Lyonnet, S
Vekemans, M
Carter, N P
Munnich, A
Colleaux, L
Cormier-Daire, V - Abstract:
- Is Part Of:
- Journal of medical genetics. Volume 41:Issue 12(2004)
- Journal:
- Journal of medical genetics
- Issue:
- Volume 41:Issue 12(2004)
- Issue Display:
- Volume 41, Issue 12 (2004)
- Year:
- 2004
- Volume:
- 41
- Issue:
- 12
- Issue Sort Value:
- 2004-0041-0012-0000
- Page Start:
- e128
- Page End:
- e128
- Publication Date:
- 2004-12-09
- Subjects:
- CdLS, Cornelia de Lange syndrome -- DAPI, 4′, 6′-diamidino-2-phenylindole
array-CGH -- Brachmann de Lange syndrome -- isochromosome 18p -- NIPBL -- subtelomeric deletion
Medical genetics -- Periodicals
616.042 - Journal URLs:
- http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/jmg.2004.026666 ↗
- Languages:
- English
- ISSNs:
- 1468-6244
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 19139.xml