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	1.	Protoporphyrinogen oxidase: complete genomic sequence and polymorphisms in the human gene. [electronic resource] by Puy, H Robréau, A M Rosipal, R Nordmann, Y Deybach, J C Producer: 19961022 In: Biochemical and biophysical research communications vol. 226 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Detection of four novel mutations in the porphobilinogen deaminase gene in French Caucasian patients with acute intermittent porphyria. [electronic resource] by Puy, H Deybach, J C Lamoril, J Robreau, A M Nordmann, Y Producer: 19970311 In: Human heredity vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Acute intermittent porphyria: rapid molecular diagnosis. [electronic resource] by Puy, H Aquaron, R Lamoril, J Robréau, A M Nordmann, Y Deybach, J C Producer: 19970708 In: Cellular and molecular biology (Noisy-le-Grand, France) vol. 43 Availability: No items available. Save to lists Add to cart (remove)
	4.	Comprehensive cytochrome P450 CYP1A2 gene analysis in French caucasian patients with familial and sporadic porphyria cutanea tarda. [electronic resource] by Tchernitchko, D Robréau, A M Lefebvre, T Lamoril, J Deybach, J C Puy, H Producer: 20120327 In: The British journal of dermatology vol. 166 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Exon 1 donor splice site mutations in the porphobilinogen deaminase gene in the non-erythroid variant form of acute intermittent porphyria. [electronic resource] by Puy, H Gross, U Deybach, J C Robréau, A M Frank, M Nordmann, Y Doss, M Producer: 19990112 In: Human genetics vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Mutations in the protoporphyrinogen oxidase gene in patients with variegate porphyria. [electronic resource] by Deybach, J C Puy, H Robréau, A M Lamoril, J Da Silva, V Grandchamp, B Nordmann, Y Producer: 19970113 In: Human molecular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	New mutations of the hydroxymethylbilane synthase gene in German patients with acute intermittent porphyria. [electronic resource] by Gross, U Puy, H Doss, M Robreau, A M Nordmann, Y Doss, M O Deybach, J C Producer: 20000225 In: Molecular and cellular probes vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Molecular epidemiology and diagnosis of PBG deaminase gene defects in acute intermittent porphyria. [electronic resource] by Puy, H Deybach, J C Lamoril, J Robreau, A M Da Silva, V Gouya, L Grandchamp, B Nordmann, Y Producer: 19970710 In: American journal of human genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Evaluation of mutation screening by heteroduplex analysis in acute intermittent porphyria: comparison with denaturing gradient gel electrophoresis. [electronic resource] by Tchernitchko, D Lamoril, J Puy, H Robreau, A M Bogard, C Rosipal, R Gouya, L Deybach, J C Nordmann, Y Producer: 19990504 In: Clinica chimica acta; international journal of clinical chemistry vol. 279 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Acute intermittent porphyria: prevalence of mutations in the porphobilinogen deaminase gene in blood donors in France. [electronic resource] by Nordmann, Y Puy, H Da Silva, V Simonin, S Robreau, A M Bonaiti, C Phung, L N Deybach, J C Producer: 19971118 In: Journal of internal medicine vol. 242 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Variegate porphyria in Western Europe: identification of PPOX gene mutations in 104 families, extent of allelic heterogeneity, and absence of correlation between phenotype and type of mutation. [electronic resource] by Whatley, S D Puy, H Morgan, R R Robreau, A M Roberts, A G Nordmann, Y Elder, G H Deybach, J C Producer: 20001002 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Loss of heterozygosity on 10q and mutational status of PTEN and BMPR1A in colorectal primary tumours and metastases. [electronic resource] by Karoui, M Tresallet, C Julie, C Zimmermann, U Staroz, F Brams, A Muti, C Boulard, C Robreau, A-M Puy, H Malafosse, R Penna, C Pruvot, F-R Thiery, J P Boileau, C Rougier, P Nordlinger, B Radvanyi, F Franc, B Hofmann-Radvanyi, H Producer: 20040422 In: British journal of cancer vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)