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	1.	Acromelic frontonasal dysostosis and ZSWIM6 mutation: phenotypic spectrum and mosaicism. [electronic resource] by Twigg, S R F Ousager, L B Miller, K A Zhou, Y Elalaoui, S C Sefiani, A Bak, G S Hove, H Hansen, L K Fagerberg, C R Tajir, M Wilkie, A O M Producer: 20170630 In: Clinical genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Search for ReCQL4 mutations in 39 patients genotyped for suspected Rothmund-Thomson/Baller-Gerold syndromes. [electronic resource] by Piard, J Aral, B Vabres, P Holder-Espinasse, M Mégarbané, A Gauthier, S Capra, V Pierquin, G Callier, P Baumann, C Pasquier, L Baujat, G Martorell, L Rodriguez, A Brady, A F Boralevi, F González-Enseñat, M A Rio, M Bodemer, C Philip, N Cordier, M-P Goldenberg, A Demeer, B Wright, M Blair, E Puzenat, E Parent, P Sznajer, Y Francannet, C DiDonato, N Boute, O Barlogis, V Moldovan, O Bessis, D Coubes, C Tardieu, M Cormier-Daire, V Sousa, A B Franques, J Toutain, A Tajir, M Elalaoui, S C Geneviève, D Thevenon, J Courcet, J-B Rivière, J-B Collet, C Gigot, N Faivre, L Thauvin-Robinet, C Producer: 20151022 In: Clinical genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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