1. Corpus callosum agenesis with clinically normal people caused by DCC mutations. Prenatal implication. (June 2017) Authors: Billette de Villemeur, T.; Valence, S.; Heron, D.; Heide, S.; Keren, B.; Nava, C.; des Portes, V.; Garel, C.; Blondiaux, E.; Afenjar, A.; Mignot, C.; Rastetter, A.; Depienne, C.; Moutard, M.-L. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e43 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Fetal intracerebral hemorrhage and COL4A1 mutation: promise and uncertainty. (31st January 2013) Authors: Garel, C.; Rosenblatt, J.; Moutard, M. L.; Heron, D.; Gelot, A.; Gonzales, M.; Miné, E.; Jouannic, J. M. Journal: Ultrasound in obstetrics & gynecology Issue: Volume 41:Number 2(2013:Feb.) Page Start: 228 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Fetal intracerebral hemorrhage and COL4A1 mutation: promise and uncertainty. (31st January 2013) Authors: Garel, C.; Rosenblatt, J.; Moutard, M. L.; Heron, D.; Gelot, A.; Gonzales, M.; Miné, E.; Jouannic, J. M. Journal: Ultrasound in obstetrics & gynecology Issue: Volume 41:Number 2(2013:Feb.) Page Start: 228 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genetic counselling difficulties and ethical implications of incidental findings from array‐CGH: a 7‐year national survey. Issue 5 (4th January 2016) Authors: Lefebvre, M.; Sanlaville, D.; Marle, N.; Thauvin‐Robinet, C.; Gautier, E.; Chehadeh, S.E.; Mosca‐Boidron, A.‐L.; Thevenon, J.; Edery, P.; Alex‐Cordier, M.‐P.; Till, M.; Lyonnet, S.; Cormier‐Daire, V.; Amiel, J.; Philippe, A.; Romana, S.; Malan, V.; Afenjar, A.; Marlin, S.; Chantot‐Bastaraud, S. Journal: Clinical genetics Issue: Volume 89:Issue 5(2016) Page Start: 630 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. PO-0664: Standardized Nodal Radiation (RT) through a Breast Clinical Pathway (CP) within a USA Cancer Network. (May 2017) Authors: Gebhardt, B.; Horne, Z.; Ahrendt, G.; Diego, E.; Heron, D.; Beriwal, S. Journal: Radiotherapy and oncology Issue: Volume 123:(2017:May)Supplement 1 Page Start: S347 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Truncating variants of the DLG4 gene are responsible for intellectual disability with marfanoid features. Issue 6 (14th April 2018) Authors: Moutton, S.; Bruel, A.‐L.; Assoum, M.; Chevarin, M.; Sarrazin, E.; Goizet, C.; Guerrot, A.‐M.; Charollais, A.; Charles, P.; Heron, D.; Faudet, A.; Houcinat, N.; Vitobello, A.; Tran‐Mau‐Them, F.; Philippe, C.; Duffourd, Y.; Thauvin‐Robinet, C.; Faivre, L. Journal: Clinical genetics Issue: Volume 93:Issue 6(2018) Page Start: 1172 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients. Issue 3 (4th October 2017) Authors: Chérot, E.; Keren, B.; Dubourg, C.; Carré, W.; Fradin, M.; Lavillaureix, A.; Afenjar, A.; Burglen, L.; Whalen, S.; Charles, P.; Marey, I.; Heide, S.; Jacquette, A.; Heron, D.; Doummar, D.; Rodriguez, D.; Billette de Villemeur, T.; Moutard, M.‐L.; Guët, A.; Xavier, J. Journal: Clinical genetics Issue: Volume 93:Issue 3(2018) Page Start: 567 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Whole‐exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome. Issue 2 (30th July 2015) Authors: Dimassi, S.; Labalme, A.; Ville, D.; Calender, A.; Mignot, C.; Boutry‐Kryza, N.; de Bellescize, J.; Rivier‐Ringenbach, C.; Bourel‐Ponchel, E.; Cheillan, D.; Simonet, T.; Maincent, K.; Rossi, M.; Till, M.; Mougou‐Zerelli, S.; Edery, P.; Saad, A.; Heron, D.; des Portes, V.; Sanlaville, D. Journal: Clinical genetics Issue: Volume 89:Issue 2(2016) Page Start: 198 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Wiedemann‐Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French cases. Issue 1 (17th May 2018) Authors: Baer, S.; Afenjar, A.; Smol, T.; Piton, A.; Gérard, B.; Alembik, Y.; Bienvenu, T.; Boursier, G.; Boute, O.; Colson, C.; Cordier, M.‐P.; Cormier‐Daire, V.; Delobel, B.; Doco‐Fenzy, M.; Duban‐Bedu, B.; Fradin, M.; Geneviève, D.; Goldenberg, A.; Grelet, M.; Haye, D. Journal: Clinical genetics Issue: Volume 94:Issue 1(2018) Page Start: 141 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗