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	101.	Deletion mapping of X-linked mixed deafness (DFN3) identifies a 265-525-kb region centromeric of DXS26. [electronic resource] by Dahl, N Laporte, J Hu, L Biancalana, V Le Palier, D Cohen, D Piussan, C Mandel, J L Producer: 19950515 In: American journal of human genetics vol. 56 Availability: No items available. Save to lists Add to cart (remove)
	102.	Possible person-to-person transmission of Escherichia coli O111--associated hemolytic uremic syndrome. [electronic resource] by Boudailliez, B Berquin, P Mariani-Kurkdjian, P Ilef, D Cuvelier, B Capek, I Tribout, B Bingen, E Piussan, C Producer: 19970515 In: Pediatric nephrology (Berlin, Germany) vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	103.	The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21). [electronic resource] by Saugier-Veber, P Abadie, V Moncla, A Mathieu, M Piussan, C Turleau, C Mattei, J F Munnich, A Lyonnet, S Producer: 19930701 In: American journal of human genetics vol. 52 Availability: No items available. Save to lists Add to cart (remove)
	104.	Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2. [electronic resource] by Biancalana, V Briard, M L David, A Gilgenkrantz, S Kaplan, J Mathieu, M Piussan, C Poncin, J Schinzel, A Oudet, C Producer: 19920526 In: American journal of human genetics vol. 50 Availability: No items available. Save to lists Add to cart (remove)
	105.	[Juvenile chronic arthritis. Double-blind study of the efficacy and tolerance of D-penicillamine]. [electronic resource] by Prieur, A M Piussan, C Manigne, P Bordigoni, P Griscelli, C Reinert, P de Goujon, F Lefur, J M Garnier, J M Producer: 19850628 In: Archives francaises de pediatrie vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	106.	[African trypanosomiasis in children treated with eflornithine. A case]. [electronic resource] by Benhamou, P H Chandenier, J Schechter, P J Epelbaum, S Tell, G P Haegele, K D Pautard, J C Piussan, C Producer: 19890810 In: Presse medicale (Paris, France : 1983) vol. 18 Availability: No items available. Save to lists Add to cart (remove)
	107.	[ Chronic juvenile arthritis. Double-blind study of efficacy and tolerance of D-penicillamine]. [electronic resource] by Prieur, A M Piussan, C Manigne, P Bordigoni, P Griscelli, C Reinert, P de Goujon, F Lefur, J M Garnier, J M Producer: 19860527 In: Revue du rhumatisme et des maladies osteo-articulaires vol. 53 Availability: No items available. Save to lists Add to cart (remove)
	108.	Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome. [electronic resource] by Yu, C E Oshima, J Goddard, K A Miki, T Nakura, J Ogihara, T Poot, M Hoehn, H Fraccaro, M Piussan, C Producer: 19940815 In: American journal of human genetics vol. 55 Availability: No items available. Save to lists Add to cart (remove)
	109.	The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28. [electronic resource] by Smahi, A Hyden-Granskog, C Peterlin, B Vabres, P Heuertz, S Fulchignoni-Lataud, M C Dahl, N Labrune, P Le Marec, B Piussan, C Producer: 19940718 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	110.	Homozygosity mapping of the Werner syndrome locus (WRN). [electronic resource] by Nakura, J Wijsman, E M Miki, T Kamino, K Yu, C E Oshima, J Fukuchi, K Weber, J L Piussan, C Melaragno, M I Producer: 19950314 In: Genomics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	111.	[An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia]. [electronic resource] by Szpiro-Tapia, S Kaplan, J Pelet, A Guilloud-Bataille, M Heuertz, S Nivelon-Chevallier, A Mathieu, M Piussan, C Journel, H Dodinval, P Producer: 19900425 In: Annales de pediatrie vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	112.	Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers. [electronic resource] by Goddard, K A Yu, C E Oshima, J Miki, T Nakura, J Piussan, C Martin, G M Schellenberg, G D Wijsman, E M Producer: 19960725 In: American journal of human genetics vol. 58 Availability: No items available. Save to lists Add to cart (remove)
	113.	Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families. [electronic resource] by Elbaz, A Vale-Santos, J Jurkat-Rott, K Lapie, P Ophoff, R A Bady, B Links, T P Piussan, C Vila, A Monnier, N Producer: 19950309 In: American journal of human genetics vol. 56 Availability: No items available. Save to lists Add to cart (remove)
	114.	Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group. [electronic resource] by Yu, C E Oshima, J Wijsman, E M Nakura, J Miki, T Piussan, C Matthews, S Fu, Y H Mulligan, J Martin, G M Schellenberg, G D Producer: 19970213 In: American journal of human genetics vol. 60 Availability: No items available. Save to lists Add to cart (remove)
	115.	Polymorphisms at the Werner locus: I. Newly identified polymorphisms, ethnic variability of 1367Cys/Arg, and its stability in a population of Finnish centenarians. [electronic resource] by Castro, E Ogburn, C E Hunt, K E Tilvis, R Louhija, J Penttinen, R Erkkola, R Panduro, A Riestra, R Piussan, C Deeb, S S Wang, L Edland, S D Martin, G M Oshima, J Producer: 19990517 In: American journal of medical genetics vol. 82 Availability: No items available. Save to lists Add to cart (remove)
	116.	Homozygous and compound heterozygous mutations at the Werner syndrome locus. [electronic resource] by Oshima, J Yu, C E Piussan, C Klein, G Jabkowski, J Balci, S Miki, T Nakura, J Ogihara, T Ells, J Smith, M Melaragno, M I Fraccaro, M Scappaticci, S Matthews, J Ouais, S Jarzebowicz, A Schellenberg, G D Martin, G M Producer: 19970314 In: Human molecular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	117.	Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children). [electronic resource] by Mathieu, M Piussan, C Thepot, F Gouget, A Lacombe, D Pedespan, J M Serville, F Fontan, D Ruffie, M Nivelon-Chevallier, A Amblard, F Chauveau, P Moirot, H Chabrolle, J P Croquette, M F Teyssier, M Plauchu, H Pelissier, M C Gilgenkrantz, S Turc-Carel, C Turleau, C Prieur, M Le Merrer, M Gonzales, M Journel, H Producer: 19970610 In: Annales de genetique vol. 40 Availability: No items available. Save to lists Add to cart (remove)

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