Results of search for 'au:"BOUE, A"' › مکتبة رقمیه للعلوم الطبيه catalog

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	241.	First-trimester free beta (hCG) screening for Down syndrome. [electronic resource] by Macri, J N Spencer, K Aitken, D Garver, K Buchanan, P D Muller, F Boue, A Producer: 19931123 In: Prenatal diagnosis vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	242.	FRAXAC2 instability. [electronic resource] by Mornet, E Chateau, C Taillandier, A Montagnon, M Simon-Bouy, B Serre, J L Boué, A Producer: 19941109 In: Nature genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	243.	Do racial differences exist in second-trimester maternal hCG levels? A study of 23,369 patients. [electronic resource] by Muller, F Bussières, L Pèlissier, M C Oury, J F Boué, C Uzan, S Boué, A Producer: 19941216 In: Prenatal diagnosis vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	244.	Prenatal exclusion of congenital erythropoietic porphyria (Günther's disease) in a fetus at risk. [electronic resource] by Deybach, J C Grandchamp, B Grelier, M Nordmann, Y Boué, J Boué, A de Berrianger, P Producer: 19800514 In: Human genetics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	245.	Gene dosage effect in human triploid fibroblasts. [electronic resource] by Junien, C Rubinson, H Dreyfus, J C Meinenhofer, M C Ravise, N Boué, J Boué, A Producer: 19760925 In: Human genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	246.	Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: first report of two cases. [electronic resource] by Junien, C Leroux, A Lostanlen, D Reghis, A Boue, J Nicolas, H Boue, A Kaplan, J C Producer: 19821021 In: Prenatal diagnosis vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	247.	[In vitro study of fibroblasts from patients with Duchenne muscular dystrophy. Evaluation of capping and ultrastructural aspect]. [electronic resource] by Charbonné, F Perissel, B Boué, A Normand, B Mage, G Vanneuville, G Turchini, J P Malet, P Producer: 19860214 In: Pathologie-biologie vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	248.	HLA-A, B, C, DR alleles in congenital adrenal hyperplasia. [electronic resource] by Couillin, P Kottler-Missonnier, M L Grisard, M C Hors, J Feingold, J Boué, J Boué, A Producer: 19800712 In: Human genetics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	249.	Simultaneous determination of the camptothecin analogue CPT-11 and its active metabolite SN-38 by high-performance liquid chromatography: application to plasma pharmacokinetic studies in cancer patients. [electronic resource] by Barilero, I Gandia, D Armand, J P Mathieu-Boué, A Ré, M Gouyette, A Chabot, G G Producer: 19920814 In: Journal of chromatography vol. 575 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	250.	Neutralization epitope patterns of poliovirus strains isolated from paralytic cases. [electronic resource] by Crainic, R Blondel, B Aubert-Combiescu, A Beytout, D Couillin, P Candrea, A Boué, A Horaud, F Producer: 19850328 In: Developments in biological standardization vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	251.	PK3: a new chromosome enzyme marker for gene dosage studies in chromosome 15 imbalance. [electronic resource] by Junien, C Rubinson-Skala, H Dreyfus, J C Ravise, N Boué, J Boué, A Kaplan, J C Producer: 19800923 In: Human genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	252.	Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency. [electronic resource] by Mornet, E Crété, P Kuttenn, F Raux-Demay, M C Boué, J White, P C Boué, A Producer: 19910205 In: American journal of human genetics vol. 48 Availability: No items available. Save to lists Add to cart (remove)
	253.	Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probes. [electronic resource] by Raux-Demay, M Mornet, E Boue, J Couillin, P Oury, J F Ravise, N Deluchat, C Boue, A Producer: 19891003 In: Prenatal diagnosis vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	254.	Genetic differences between cystic fibrosis with and without meconium ileus. [electronic resource] by Mornet, E Simon-Bouy, B Serre, J L Estivill, X Farrall, M Williamson, R Boue, J Boue, A Producer: 19880323 In: Lancet (London, England) vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	255.	Therapeutic efficacy of the topoisomerase I inhibitor 7-ethyl-10-(4-[1-piperidino]-1-piperidino)-carbonyloxy-camptothecin against human tumor xenografts: lack of cross-resistance in vivo in tumors with acquired resistance to the topoisomerase I inhibitor 9-dimethylaminomethyl-10-hydroxycamptothecin. [electronic resource] by Houghton, P J Cheshire, P J Hallman, J C Bissery, M C Mathieu-Boué, A Houghton, J A Producer: 19930707 In: Cancer research vol. 53 Availability: No items available. Save to lists Add to cart (remove)
	256.	Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probes. [electronic resource] by Mornet, E Simon-Bouy, B Serre, J L Muller, F Taillandier, A Martinez, M Boue, J Boue, A Producer: 19890627 In: Clinical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	257.	Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency. [electronic resource] by Mornet, E Couillin, P Kutten, F Raux, M C White, P C Cohen, D Boué, A Dausset, J Producer: 19870211 In: Human genetics vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	258.	Prenatal diagnosis in 200 pregnancies with a 1-in-4 risk of cystic fibrosis. [electronic resource] by Boué, A Muller, F Nezelof, C Oury, J F Duchatel, F Dumez, Y Aubry, M C Boué, J Producer: 19870120 In: Human genetics vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	259.	Workshop on collaborative studies in prenatal diagnosis of chromosome disease. [electronic resource] by Hamerton, J Boué, A Ferguson-Smith, M Hsu, L Lindsten, J Mikkelsen, M Stene, J Warburton, D Worton, R Producer: 19830415 In: Progress in clinical and biological research vol. 103 Pt B Availability: No items available. Save to lists Add to cart (remove)
	260.	Maternal serum free beta hCG screening: results of studies including 480 cases of Down syndrome. [electronic resource] by Macri, J N Spencer, K Garver, K Buchanan, P D Say, B Carpenter, N J Muller, F Boué, A Producer: 19940616 In: Prenatal diagnosis vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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