Frequency of the cystic fibrosis mutation ΔF508 in Algeria von LUCOTTE, G, BARRE, E, BERRICHE, S

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Cerebral Aneurysms : A Rare Feature of Behçet's Disease—A Case Report and Review of the Literature von Younes, Samia, Cherif, Yosra, Mokni, Narjes, Berriche, Olfa, Zantour, Baha, Boughammoura, Amel, Frih-Ayed, Mahbouba, Jerbi, Saida, Sfar, Mohamed Habib

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A recombinant Friedreich's ataxia family von LUCOTTE, G, BERRICHE, S, TURPIN, J. C

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Linkage analysis of French families with facioscapulohumeral muscular dystrophy von Lucotte, G, Berriche, S, Fardeau, M

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A multiple primer pairs polymerase chain reaction for the detection of human genital papillomavirus types von Lucotte, G., François, M.-H., Petit, M.-C., Berriche, S., Réveilleau, S.

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Familial adrenoleukodystrophy: long chain fatty acid levels and analysis with a factor VIII DNA probe von BERRICHE, S, TURPIN, J. C, LUCOTTE, G

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Y-chromosome DNA Haplotypes in North African Populations von LUCOTTE, GÉRARD, AOUIZÉRATE, ANNIE, BERRICHE, SALA

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Haplotype VIII of the Y Chromosome Is the Ancestral Haplotype in Jews von LUCOTTE, GÉRARD, DAVID, FABRICE, BERRICHE, SALA

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Association of apolipoprotein E allele ϵ4 with late-onset sporadic Alzheimer's disease von Lucotte, G., Visvikis, S., Leininger-Möler, B., David, F., Berriche, S., Revéilleau, S., Couderc, R., Babron, M. C., Aguillon, D., Siest, G.

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Alzheimer's mutation von LUCOTTE, GERARD, BERRICHE, SALA, DAVID, FABRìCE

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Frequency of the cystic fibrosis mutation ?F508 in Algeria von Lucotte, G., Barr, E., Berriche, S.

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Utilisation du polymorphisme Pvull de la région d'ADN hypervariable située en 3′ du gène α-globine aux problèmes d'exclusion de paternité von Lucotte, G, Berriche, S

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Les techniques de polymorphismes de l'A.D.N. de sondes du chromosome Y appliquées au problème de filiations père-fils dans les analyses de paternité von Guérin, P., Berriche, S., Intrator, S., Rouger, Ph, Salmon, D., Salmon, Ch, Lucotte, G.

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Effect of Thyroid Hormones and Cyclic AMP on Some Lipogenic Enzymes of the Fat Cell von CORREZE, Claude, BERRICHE, Salahedine, TAMAYO, Libardo, NUNEZ, Jacques

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Association of apolipoprotein E allele epsilon 4 with late-onset sporadic Alzheimer's disease von Lucotte, G, Visvikis, S, Leininger-Müler, B, David, F, Berriche, S, Réveilleau, S, Couderc, R, Babron, M C, Aguillon, D, Siest, G

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Détection des mutations de la mucoviscidose dans les familles de la région parisienne von Lucotte, G., Berriche, S., David, F., Reveilleau, S., Lu, C.Y., Bathelier, C., Champenois, T.

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Techniques of DNA polymorphisms revealed by probes for the Y chromosome applied to questions of father-son line in analyses of paternity von Guérin, P, Berriche, S, Intrator, S, Rouger, P, Salmon, D, Salmon, C, Lucotte, G

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Comparative Study of Fingerprint-Based Gender Identification von Berriche, Lamia

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Misinformation on Misinformation: Conceptual and Methodological Challenges von Altay, Sacha, Berriche, Manon, Acerbi, Alberto

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Hugo MERCIER, Not born yesterday: The science of who we trust and what we believe. Princeton, NJ, Princeton University Press, 2020, 384 p von Berriche, Manon

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