Critical Role of the D21S55 Region on Chromosome 21 in the Pathogenesis of Down Syndrome
Rahmani, Zohra, Blouin, Jean-Louis, Creau-Goldberg, Nicole, Watkins, Paul C., Mattei, Jean-François, Poissonnier, Marc, Prieur, Marguerite, Chettouh, Zoubida, Nicole, Annie, Aurias, Alain, Sinet, Pierre-Marie, Delabar, Jean-Maurice
Published in Proceedings of the National Academy of Sciences - PNAS (01.08.1989)
Published in Proceedings of the National Academy of Sciences - PNAS (01.08.1989)
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Mapping of the human retinoic acid receptor to the q21 band of chromosome 17
Mattei, M G, Petkovich, M, Mattei, J F, Brand, N, Chambon, P
Published in Human genetics (01.10.1988)
Published in Human genetics (01.10.1988)
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Journal Article
Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counselling
Moncla, Anne, Malzac, Perrine, Livet, Marie-Odile, Voelckel, Marie-Antoinette, Mancini, Josette, Delaroziere, Jean Christophe, Philip, Nicole, Mattei, Jean-François
Published in Journal of medical genetics (01.07.1999)
Published in Journal of medical genetics (01.07.1999)
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Journal Article
XNP mutation in a large family with Juberg-Marsidi syndrome
Munnich, Arnold, Villard, Laurent, Gecz, Josef, Lyonnet, Stanislas, Fontés, Michel, Mattéi, Jean François, Saugier-Veber, Pascale
Published in Nature genetics (01.04.1996)
Published in Nature genetics (01.04.1996)
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Outcome of a school screening programme for carriers of haemoglobin disease
Lena-Russo, D, Badens, C, Aubinaud, M, Merono, F, Paolasso, C, Martini, N, Mattei, J F
Published in Journal of medical screening (01.01.2002)
Published in Journal of medical screening (01.01.2002)
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Journal Article
DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome
Mattei, M G, Philip, N, Passage, E, Moisan, J P, Mandel, J L, Mattei, J F
Published in Human genetics (01.03.1985)
Published in Human genetics (01.03.1985)
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Journal Article
The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice
Dautigny, A, Mattei, M G, Morello, D, Alliel, P M, Pham-Dinh, D, Amar, L, Arnaud, D, Simon, D, Mattei, J F, Guenet, J L
Published in Nature (London) (26.06.1986)
Published in Nature (London) (26.06.1986)
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Humanity and human DNA
Mattei, J-F
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.03.2013)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.03.2013)
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Journal Article
Localization of the Human NCAM Gene to Band q23 of Chromosome 11: The Third Gene Coding for a Cell Interaction Molecule Mapped to the Distal Portion of the Long Arm of Chromosome 11
Nguyen, Catherine, Mattei, Marie-Geneviève, Mattei, Jean-François, Santoni, Marie-José, Goridis, Christo, Jordan, Bertrand R.
Published in The Journal of cell biology (01.03.1986)
Published in The Journal of cell biology (01.03.1986)
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De l’homme et son ADN
Mattei, J.-F.
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.03.2013)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.03.2013)
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Journal Article
A first molecular approach towards CGG repeat expansion in FMR1 gene in systemic lupus erythematosus and in Sjögren's syndrome: a preliminary report
Granel, B, Ravix, V, Pedeillier, K, Serratrice, J, Disdier, P, Voelckel, M A, Mattei, J F, Weiller, P J
Published in Clinical rheumatology (01.01.2000)
Published in Clinical rheumatology (01.01.2000)
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Journal Article
Genetic Services in France
Aymé, S., Briard, M.-L., Mattei, J.-F.
Published in European journal of human genetics : EJHG (01.01.1997)
Published in European journal of human genetics : EJHG (01.01.1997)
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Journal Article
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male
Camerino, G, Mattei, M G, Mattei, J F, Jaye, M, Mandel, J L
Published in Nature (London) (01.01.1983)
Published in Nature (London) (01.01.1983)
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The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21)
SAUGIER-VEBER, P, ABADIE, V, MONCLA, A, MATHIEU, M, PIUSSAN, C, TURLEAU, C, MATTEI, J.-F, MUNNICH, A, LYONNET, S
Published in American journal of human genetics (01.06.1993)
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Published in American journal of human genetics (01.06.1993)
Journal Article
Physicians' acceptability of termination of pregnancy after prenatal diagnosis in southern France
Julian, C, Huard, P, Gouvernet, J, Mattéi, J F, Aymé, S
Published in Prenatal diagnosis (01.02.1989)
Published in Prenatal diagnosis (01.02.1989)
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Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new cases
Moncla, A, Livet, M O, Auger, M, Mattei, J F, Mattei, M G, Giraud, F
Published in Journal of medical genetics (01.09.1991)
Published in Journal of medical genetics (01.09.1991)
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Journal Article
CpG dinucleotides are mutation hot spots in phenylketonuria
Abadie, Véronique, Lyonnet, Stanislas, Maurin, Nicole, Berthelon, Monique, Caillaud, Catherine, Giraud, Francis, Mattei, Jean-François, Rey, Jean, Rey, Françoise, Munnich, Arnold
Published in Genomics (San Diego, Calif.) (01.11.1989)
Published in Genomics (San Diego, Calif.) (01.11.1989)
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