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1دورية أكاديمية
المؤلفون: Noruzinia Mehrdad, Lefort Genevieve, Chaze Anne Marie, Puechberty Jacques, Pellestor Franck, Blanchet Patricia, Cacheux Valerie, Sarda Pierre
المصدر: Acta Medica Iranica, Vol 47, Iss 3, Pp 233-240 (2009)
مصطلحات موضوعية: Chromosome 16, pure partial trisomy, interstitial duplication, Medicine (General), R5-920
وصف الملف: electronic resource
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2دورية أكاديمية
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3دورية أكاديمية
المؤلفون: Roizès Gérard, Puechberty Jacques, Pironon Nathalie
المصدر: BMC Genomics, Vol 11, Iss 1, p 195 (2010)
مصطلحات موضوعية: Biotechnology, TP248.13-248.65, Genetics, QH426-470
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Pagès Michel, Crobu Lucien, Meghamla Sabrina, Blaineau Christine, Puechberty Jacques, Bastien Patrick
المصدر: BMC Genomics, Vol 8, Iss 1, p 57 (2007)
مصطلحات موضوعية: Biotechnology, TP248.13-248.65, Genetics, QH426-470
وصف الملف: electronic resource
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5دورية أكاديمية
المؤلفون: Schanze, Ina, Bunt, Jens, Lim, Jonathan WC, Schanze, Denny, Dean, Ryan J, Alders, Marielle, Blanchet, Patricia, Attié-Bitach, Tania, Berland, Siren, Boogert, Steven, Boppudi, Sangamitra, Bridges, Caitlin J, Cho, Megan T, Dobyns, William B, Donnai, Dian, Douglas, Jessica, Earl, Dawn L, Edwards, Timothy J, Faivre, Laurence, Fregeau, Brieana, Genevieve, David, Gérard, Marion, Gatinois, Vincent, Holder-Espinasse, Muriel, Huth, Samuel F, Izumi, Kosuke, Kerr, Bronwyn, Lacaze, Elodie, Lakeman, Phillis, Mahida, Sonal, Mirzaa, Ghayda M, Morgan, Sian M, Nowak, Catherine, Peeters, Hilde, Petit, Florence, Pilz, Daniela T, Puechberty, Jacques, Reinstein, Eyal, Rivière, Jean-Baptiste, Santani, Avni B, Schneider, Anouck, Sherr, Elliott H, Smith-Hicks, Constance, Wieland, Ilse, Zackai, Elaine, Zhao, Xiaonan, Gronostajski, Richard M, Zenker, Martin, Richards, Linda J
المصدر: American Journal of Human Genetics. 103(5)
مصطلحات موضوعية: Biomedical and Clinical Sciences, Mental Health, Pediatric, Intellectual and Developmental Disabilities (IDD), Neurosciences, Rare Diseases, Behavioral and Social Science, Genetics, Brain Disorders, Aetiology, 2.1 Biological and endogenous factors, Mental health, Neurological, Adolescent, Adult, Animals, Cerebral Cortex, Child, Child, Preschool, Codon, Nonsense, Cohort Studies, Corpus Callosum, Female, Haploinsufficiency, Humans, Intellectual Disability, Male, Megalencephaly, Mice, Mice, Knockout, NFI Transcription Factors, Polymorphism, Single Nucleotide, Young Adult, NFIB, agenesis of the corpus callosum, chromosome 9p22.3, chromosome 9p23, developmental delay, haploinsufficiency, intellectual disability, macrocephaly, megalencephaly, nuclear factor I, Biological Sciences, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/7099p72x
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6دورية أكاديمية
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7دورية أكاديمية
المؤلفون: Celse, TristanAff1, Aff2, Cazin, CarolineAff1, Aff2, Mietton, Flore, Martinez, GuillaumeAff1, Aff3, Martinez, Delphine, Thierry-Mieg, Nicolas, Septier, Amandine, Guillemain, CatherineAff5, Aff6, Beurois, Julie, Clergeau, Antoine, Mustapha, Selima Fourati Ben, Kharouf, Mahmoud, Zoghmar, Abdelali, Chargui, Ahmed, Papaxanthos, Aline, Dorphin, Béatrice, Foliguet, Bernard, Triki, Chema, Sifer, Christophe, Lauton, Dominique, Tachdjian, Gérard, Schuler, Gilles, Lejeune, Hervé, Puechberty, Jacques, Bessonnat, Julien, Pasquier, Laurent, Mery, Lionel, Poulain, Marine, Chaabouni, Myriam, Sermondade, Nathalie, Cabry, Rosalie, Benbouhadja, Sebti, Veau, Ségolène, Frapsauce, Cynthia, Mitchell, Valérie, Achard, VincentAff30, Aff31, Aff32, Satre, VeroniqueAff1, Aff3, Hennebicq, SylvianeAff1, Aff21, Zouari, Raoudha, Arnoult, Christophe, Kherraf, Zine-EddineAff1, Aff2, Coutton, CharlesAff1, Aff3, Ray, Pierre F.Aff1, Aff2
المصدر: Human Genetics. 140(1):43-57
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8دورية أكاديمية
المؤلفون: Ban, Iulian O., Chabert, Alice, Guignard, Thomas, Puechberty, Jacques, Cabello-Aguilar, Simon, Pujol, Pascal, Vendrell, Julie A., Solassol, Jérôme
المصدر: Frontiers in Oncology; 2024, p1-7, 7p
مصطلحات موضوعية: TRIPLE-negative breast cancer, HOMOLOGOUS recombination, PHENOTYPIC plasticity, SEQUENCE analysis
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9دورية أكاديمية
المؤلفون: Nguyen, Ngoc Minh Phuong 1, Khawajkie, Yassemine 2, Mechtouf, Nawel 1, Rezaei, Maryam 1, Breguet, Magali 3, Kurvinen, Elvira 4, Jagadeesh, Sujatha 5, Solmaz, Asli Ece 6, Aguinaga, Monica 7, Hemida, Reda 8, Harma, Mehmet Ibrahim 9, Rittore, Cécile 10, Rahimi, Kurosh 11, Arseneau, Jocelyne 12, Hovanes, Karine 13, Clisham, Ronald 14, Lenzi, Tiffanee 15, Scurry, Bonnie 16, Addor, Marie-Claude 17, Bagga, Rashmi 18, Nendaz, Genevieve Girardet 19, Finci, Vildana 20, Poke, Gemma 21, Grimes, Leslie 22, Gregersen, Nerine 23, York, Kayla 24, Bolze, Pierre-Adrien 25, Patel, Chirag 26, Mozdarani, Hossein 27, Puechberty, Jacques 28, Scotchie, Jessica 29, Fardaei, Majid 30, Harma, Muge 9, Gardner, R. J. McKinlay 21, 31, Sahoo, Trilochan 13, Dudding-Byth, Tracy 32, Srinivasan, Radhika 33, Sauthier, Philippe 3, Slim, Rima 1, 2, 31
المصدر: In Modern Pathology July 2018 31(7):1116-1130
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10دورية أكاديمية
المؤلفون: Cayrefourcq, Laure, Vincent, Marie-Claire, Pierredon, Sandra, Moutou, Céline, Imbert-Bouteille, Marion, Haquet, Emmanuelle, Puechberty, Jacques, Willems, Marjolaine, Liautard-Haag, Cathy, Molinari, Nicolas, Zordan, Cécile, Dorian, Virginie, Rooryck-Thambo, Caroline, Goizet, Cyril, Chaussenot, Annabelle, Rouzier, Cécile, Boureau-Wirth, Amandine, Monteil, Laetitia, Calvas, Patrick, Miry, Claire, Favre, Romain, Petrov, Yuliya, Khau Van Kien, Philippe, Le Boette, Elsa, Fradin, Mélanie, Alix-Panabières, Catherine, Guissart, ClaireAff1
المصدر: Scientific Reports. 10(1)