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Association of an HLA-DQ Allele With Clinical Tuberculosis
Goldfeld, Anne E, Delgado, Julio C, Thim, Sok, Bozon, M. Viviana, Uglialoro, Adele M, Turbay, David, Cohen, Carol, Yunis, Edmond J
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A Locus for Autosomal Dominant Colobomatous Microphthalmia Maps to Chromosome 15q12-q15
Morlé, L., Bozon, M., Zech, J.-C., Alloisio, N., Raas-Rothschild, A., Philippe, C., Lambert, J.-C., Godet, J., Plauchu, H., Edery, P.
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A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss
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Frequent de novo mutations of the ANK1 gene mimic a recessive mode of transmission in hereditary spherocytosis: three new ANK1 variants: ankyrins Bari, Napoli II and Anzio
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Changes in sexual behaviours: from secular trends to public health policies
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A Deletional Frameshift Mutation in Protein 4.2 Gene (Allele 4.2 Lisboa) Associated With Hereditary Hemolytic Anemia
Hayette, S., Dhermy, D., Dos Santos, M.-E., Bozon, M., Drenckhahn, D., Alloisio, N., Texier, P., Delaunay, J., Morlέ, L.
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Ankyrin Napoli: a de novo deletional frameshift mutation in exon 16 of ankyrin gene (ANK1) associated with spherocytosis
del Giudice, E M, Hayette, S, Bozon, M, Perrotta, S, Alloisio, N, Vallier, A, Iolascon, A, Delaunay, J, Morlé, L
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Published in British journal of haematology (01.06.1996)
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A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemia
Hayette, S, Morle, L, Bozon, M, Ghanem, A, Risinger, M, Korsgren, C, Tanner, M J, Fattoum, S, Cohen, C M, Delaunay, J
Published in British journal of haematology (01.04.1995)
Published in British journal of haematology (01.04.1995)
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Two distinct truncated variants of ankyrin associated with hereditary spherocytosis
Hayette, S., Carré, G., Bozon, M., Alloisio, N., Maillet, P., Wilmotte, R., Pascal, O., Reynaud, J., Reman, O., Stéphan, J.‐L., Morlé, L., Delaunay, J.
Published in American journal of hematology (01.05.1998)
Published in American journal of hematology (01.05.1998)
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Ankyrin Bugey: A de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis
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Transmission génétique de la cataracte congénitale
BEBY, F, MORLE, L, MICHON, L, BOZON, M, EDERY, P, BURILLON, C, DENIS, Ph
Published in Journal français d'ophtalmologie (01.04.2003)
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MHC class II alleles and haplotypes in patients with pemphigus vulgaris from India
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Published in Tissue antigens (01.12.1996)
Published in Tissue antigens (01.12.1996)
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Comparison of HLA-A antigen typing by serology with two polymerase chain reaction based DNA typing methods: implications for proficiency testing
Bozón, M V, Delgado, J C, Turbay, D, Salazar, M, Granja, C B, Alosco, S M, Dupont, B, Yunis, E J
Published in Tissue antigens (01.06.1996)
Published in Tissue antigens (01.06.1996)
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