1. A linkage map of 10 loci flanking the Marfan syndrome locus on 15q: results of an International Consortium study. Issue 2 (February 1992) Authors: Sarfarazi, M; Tsipouras, P; Del Mastro, R; Kilpatrick, M; Farndon, P; Boxer, M; Bridges, A; Boileau, C; Junien, C; Hayward, C Journal: Journal of medical genetics Issue: Volume 29:Issue 2(1992) Page Start: 75 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females. Issue 4 (April 1992) Authors: Moutou, C; Junien, C; Henry, I; Bonaïti-Pellié, C Journal: Journal of medical genetics Issue: Volume 29:Issue 4(1992) Page Start: 217 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Congenital hyperinsulinism and mosaic abnormalities of the ploidy. Issue 3 (20th July 2005) Authors: Giurgea, I; Sanlaville, D; Fournet, J-C; Sempoux, C; Bellanné-Chantelot, C; Touati, G; Hubert, L; Groos, M-S; Brunelle, F; Rahier, J; Henquin, J-C; Dunne, M J; Jaubert, F; Robert, J-J; Nihoul-Fékété, C; Vekemans, M; Junien, C; de Lonlay, P Journal: Journal of medical genetics Issue: Volume 43:Issue 3(2006) Page Start: 248 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Linkage analysis of five fibrillar collagen loci in a large French Marfan syndrome family. Issue 2 (February 1990) Authors: Boileau, C; Jondeau, G; Bonaiti, C; Coulon, M; Delorme, G; Dubourg, O; Bourdarias, J P; Junien, C Journal: Journal of medical genetics Issue: Volume 27:Issue 2(1990) Page Start: 78 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Major difference in aetiology and phenotypic abnormalities between transient and permanent neonatal diabetes. Issue 5 (1st May 2002) Authors: Marquis, E; Robert, J J; Bouvattier, C; Bellanné-Chantelot, C; Junien, C; Diatloff-Zito, C Journal: Journal of medical genetics Issue: Volume 39:Issue 5(2002) Page Start: 370 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Misdiagnosed normal fetus owing to undetected germinal mosaicism for DMD deletion. Issue 12 (December 1989) Authors: Boileau, C; Junien, C Journal: Journal of medical genetics Issue: Volume 26:Issue 12(1989) Page Start: 790 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Prenatal diagnosis of myotonic dystrophy using closely linked flanking markers. Issue 2 (February 1991) Authors: Lavedan, C; Hofmann, H; Shelbourne, P; Duros, C; Savoy, D; Johnson, K; Junien, C Journal: Journal of medical genetics Issue: Volume 28:Issue 2(1991) Page Start: 89 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome. Issue 11 (19th November 2003) Authors: Diaz-Meyer, N; Day, C D; Khatod, K; Maher, E R; Cooper, W; Reik, W; Junien, C; Graham, G; Algar, E; Der Kaloustian, V M; Higgins, M J Journal: Journal of medical genetics Issue: Volume 40:Issue 11(2003) Page Start: 797 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗