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	1.	The mRNA transcripts from a mutant beta-globin gene derived from splicing at preferential cryptic sites. [electronic resource] by Lossi, A M Bergé-Lefranc, J L Producer: 19891204 In: FEBS letters vol. 256 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Transcript map of the human chromosome Xq11-Xq21 region: localization of 33 novel genes and one pseudogene. [electronic resource] by Villard, L Belougne, J Lossi, A M Fontés, M Colleaux, L Producer: 19990909 In: Gene vol. 235 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mutation screening of the PKD1 transcript by RT-PCR. [electronic resource] by Burtey, S Lossi, A M Bayle, J Berland, Y Fontés, M Producer: 20020708 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Physical and transcriptional mapping of DXS56-PGK1 1 Mb region: identification of three new transcripts. [electronic resource] by Gecz, J Villard, L Lossi, A M Millasseau, P Djabali, M Fontes, M Producer: 19931230 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A further case of beta-thalassemia with an homozygous T----C substitution at the donor splice site of the first intervening sequence of the beta-globin gene. [electronic resource] by Lossi, A M Milland, M Bergé-Lefranc, J L Lena-Russo, D Perrimond, H Producer: 19900215 In: Hemoglobin vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without alpha-thalassemia. [electronic resource] by Villard, L Toutain, A Lossi, A M Gecz, J Houdayer, C Moraine, C Fontès, M Producer: 19960716 In: American journal of human genetics vol. 58 Availability: No items available. Save to lists Add to cart (remove)
	7.	A polymorphic microsatellite XNP-GT in the XNP/ATRX gene's promotor allows familial indirect diagnosis. [electronic resource] by Lévy, N Bernard-Bronsard, R Lossi, A M Colleaux, L Cardoso, C Villard, L Fontés, M Producer: 19991102 In: Human mutation vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Determination of the genomic structure of the XNP/ATRX gene encoding a potential zinc finger helicase. [electronic resource] by Villard, L Lossi, A M Cardoso, C Proud, V Chiaroni, P Colleaux, L Schwartz, C Fontés, M Producer: 19970925 In: Genomics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Mutation of the XNP/ATR-X gene in a family with severe mental retardation, spastic paraplegia and skewed pattern of X inactivation: demonstration that the mutation is involved in the inactivation bias. [electronic resource] by Lossi, A M Millán, J M Villard, L Orellana, C Cardoso, C Prieto, F Fontés, M Martínez, F Producer: 19990820 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)
	10.	Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia. [electronic resource] by Philip, N Chabrol, B Lossi, A-M Cardoso, C Guerrini, R Dobyns, W B Raybaud, C Villard, L Producer: 20030707 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Exclusion of nine candidate genes for their involvement in X-linked FG syndrome (FGS1) in three families. [electronic resource] by Lossi, A M Colleaux, L Chiaroni, P Fontes, M Villard, L Abidi, F Schwartz, C Briault, S Moraine, C Producer: 20001107 In: American journal of medical genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Isolation and characterization of a repetitive DNA sequence from Leishmania infantum: development of a visceral leishmaniasis polymerase chain reaction. [electronic resource] by Piarroux, R Azaiez, R Lossi, A M Reynier, P Muscatelli, F Gambarelli, F Fontes, M Dumon, H Quilici, M Producer: 19931014 In: The American journal of tropical medicine and hygiene vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Construction of a YAC contig spanning the Xq13.3 subband. [electronic resource] by Villard, L Gecz, J Colleaux, L Lossi, A M Chelly, J Ishikawa-Brush, Y Monaco, A P Fontes, M Producer: 19950720 In: Genomics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Disruption of a new X linked gene highly expressed in brain in a family with two mentally retarded males. [electronic resource] by Cantagrel, V Lossi, A-M Boulanger, S Depetris, D Mattei, M-G Gecz, J Schwartz, C E Van Maldergem, L Villard, L Producer: 20050804 In: Journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation. [electronic resource] by Lossi, A M Laugier-Anfossi, F Depetris, D Gecz, J Gedeon, A Kooy, F Schwartz, C Mattei, M G Croquette, M F Villard, L Producer: 20020305 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1. [electronic resource] by Villard, L Briault, S Lossi, A M Paringaux, C Belougne, J Colleaux, L Pincus, D R Woollatt, E Lespinasse, J Munnich, A Moraine, C Fontès, M Gecz, J Producer: 19991119 In: Journal of medical genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndrome. [electronic resource] by Villard, L Bonino, M C Abidi, F Ragusa, A Belougne, J Lossi, A M Seaver, L Bonnefont, J P Romano, C Fichera, M Lacombe, D Hanauer, A Philip, N Schwartz, C Fontés, M Producer: 19990611 In: Journal of medical genetics vol. 36 Availability: No items available. Save to lists Add to cart (remove)