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	1.	Clinical and molecular characterization of a combined 17p13.3 microdeletion with partial monosomy 21q21.3 in a 26-year-old man. [electronic resource] by Hannachi, H Mougou-Zerelli, S BenAbdallah, I Mama, N Hamdi, I Labalme, A Elghezal, H Sanlaville, D Saad, A Producer: 20120105 In: Cytogenetic and genome research vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A novel homozygous truncating mutation of the SFRP4 gene in Pyle's disease. [electronic resource] by Chatron, N Lesca, G Labalme, A Rollat-Farnier, P A Monin, P Pichot, E Edery, P Sanlaville, D Rossi, M Producer: 20190415 In: Clinical genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	[Small animal image-guided radiotherapy: A new era for preclinical studies]. [electronic resource] by Delpon, G Frelin-Labalme, A-M Heinrich, S Beaudouin, V Noblet, C Begue, M Le Deroff, C Pouzoulet, F Chiavassa, S Producer: 20160706 In: Cancer radiotherapie : journal de la Societe francaise de radiotherapie oncologique vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Statistical method to compare massive parallel sequencing pipelines. [electronic resource] by Elsensohn, M H Leblay, N Dimassi, S Campan-Fournier, A Labalme, A Roucher-Boulez, F Sanlaville, D Lesca, G Bardel, C Roy, P Producer: 20170830 In: BMC bioinformatics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Incidental findings on array comparative genomic hybridization: detection of carrier females of dystrophinopathy without any family history. [electronic resource] by Nguyen, K Putoux, A Busa, T Cordier, M P Sigaudy, S Till, M Chabrol, B Michel-Calemard, L Bernard, R Julia, S Malzac, P Labalme, A Missirian, C Edery, P Popovici, C Philip, N Sanlaville, D Producer: 20160104 In: Clinical genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Whole-exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome. [electronic resource] by 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 Lesca, G Producer: 20161017 In: Clinical genetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Prenatal microarray comparative genomic hybridization: Experience from the two first years of activity at the Lyon university-hospital. [electronic resource] by Pons, L Till, M Alix, E Abel, C Boggio, D Bordes, A Caloone, J Raskin, F C Chatron, N Cordier, M-P Fichez, A Labalme, A Lajeunesse, C Liaras, É Massoud, M Miribel, J Ollagnon, E Schluth-Bolard, C Vichier-Cerf, A Edery, P Attia, J Huissoud, C Rudigoz, R C Massardier, J Gaucherand, P Sanlaville, D Producer: 20190710 In: Journal of gynecology obstetrics and human reproduction vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A genome-wide DNA methylation signature for SETD1B-related syndrome. [electronic resource] by Krzyzewska, I M Maas, S M Henneman, P Lip, K V D Venema, A Baranano, K Chassevent, A Aref-Eshghi, E van Essen, A J Fukuda, T Ikeda, H Jacquemont, M Kim, H-G Labalme, A Lewis, S M E Lesca, G Madrigal, I Mahida, S Matsumoto, N Rabionet, R Rajcan-Separovic, E Qiao, Y Sadikovic, B Saitsu, H Sweetser, D A Alders, M Mannens, M M A M Producer: 20200727 In: Clinical epigenetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Delineation of 15q13.3 microdeletions. [electronic resource] by Masurel-Paulet, A Andrieux, J Callier, P Cuisset, J M Le Caignec, C Holder, M Thauvin-Robinet, C Doray, B Flori, E Alex-Cordier, M P Beri, M Boute, O Delobel, B Dieux, A Vallee, L Jaillard, S Odent, S Isidor, B Beneteau, C Vigneron, J Bilan, F Gilbert-Dussardier, B Dubourg, C Labalme, A Bidon, C Gautier, A Pernes, P Pinoit, J M Huet, F Mugneret, F Aral, B Jonveaux, P Sanlaville, D Faivre, L Producer: 20101207 In: Clinical genetics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. [electronic resource] by Walters, R G Jacquemont, S Valsesia, A de Smith, A J Martinet, D Andersson, J Falchi, M Chen, F Andrieux, J Lobbens, S Delobel, B Stutzmann, F El-Sayed Moustafa, J S Chèvre, J-C Lecoeur, C Vatin, V Bouquillon, S Buxton, J L Boute, O Holder-Espinasse, M Cuisset, J-M Lemaitre, M-P Ambresin, A-E Brioschi, A Gaillard, M Giusti, V Fellmann, F Ferrarini, A Hadjikhani, N Campion, D Guilmatre, A Goldenberg, A Calmels, N Mandel, J-L Le Caignec, C David, A Isidor, B Cordier, M-P Dupuis-Girod, S Labalme, A Sanlaville, D Béri-Dexheimer, M Jonveaux, P Leheup, B Ounap, K Bochukova, E G Henning, E Keogh, J Ellis, R J Macdermot, K D van Haelst, M M Vincent-Delorme, C Plessis, G Touraine, R Philippe, A Malan, V Mathieu-Dramard, M Chiesa, J Blaumeiser, B Kooy, R F Caiazzo, R Pigeyre, M Balkau, B Sladek, R Bergmann, S Mooser, V Waterworth, D Reymond, A Vollenweider, P Waeber, G Kurg, A Palta, P Esko, T Metspalu, A Nelis, M Elliott, P Hartikainen, A-L McCarthy, M I Peltonen, L Carlsson, L Jacobson, P Sjöström, L Huang, N Hurles, M E O'Rahilly, S Farooqi, I S Männik, K Jarvelin, M-R Pattou, F Meyre, D Walley, A J Coin, L J M Blakemore, A I F Froguel, P Beckmann, J S Producer: 20100312 In: Nature vol. 463 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)