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1دورية أكاديمية
المؤلفون: Giabicani, Eloise, Willems, Marjolaine, Steunou, Virginie, Chantot-Bastaraud, Sandra, Thibaud, Nathalie, Abi Habib, Walid, Azzi, Salah, Lam, Bich, Bérard, Laurence, Bony-Trifunovic, Hélène, Brachet, Cécile, Brischoux-Boucher, Elise, Caldagues, Emmanuelle, Coutant, Regis, Cuvelier, Marie Laure, Gelwane, Georges, Guemas, Isabelle, Houang, Muriel, Isidor, Bertrand, Jeandel, Claire, Lespinasse, James, Naud-Saudreau, Catherine, Jesuran-Perelroizen, Monique, Perrin, Laurence, Piard, Juliette, Sechter, Claire, Souchon, Pierre François, Storey, Caroline, Thomas, Domitille, Le Bouc, Yves, Rossignol, Sylvie, Netchine, Irène, Brioude, Frédéric
المصدر: Journal of medical genetics
مصطلحات موضوعية: Biologie, Génétique clinique, fetal growth restriction, homozygous variant, IGF-I, IGF1R, small for gestational age
وصف الملف: 1 full-text file(s): application/pdf
العلاقة: uri/info:doi/10.1136/jmedgenet-2019-106328; uri/info:pmid/31586944; uri/info:scp/85073159461; https://dipot.ulb.ac.be/dspace/bitstream/2013/297140/3/IGF1R.pdfTest; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/297140Test
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2دورية أكاديمية
المؤلفون: Heide, Solveig, Heinrichs, Claudine, Newfield, Ron R.S., Sarda, Pierre, Van Maldergem, Lionel, Trifard, Véronique, Giabicani, Eloise, Siffroi, Jean Pierre, Le Bouc, Yves, Netchine, Irène, Brioude, Frédéric, Chantot-Bastaraud, Sandra, Keren, Boris, Harbison, Madeleine M.D., Azzi, Salah, Rossignol, Sylvie, Michot, Caroline, Lackmy-Port Lys, Marilyn, Demeer, Bénédicte
المصدر: Journal of medical genetics, 55 (3
مصطلحات موضوعية: Biologie, Génétique clinique, 11p15 Duplication, Beckwith-wiedemann Syndrome, Cnv, Imprinting Disorder, Silver Russell Syndrome
وصف الملف: 1 full-text file(s): application/pdf
العلاقة: uri/info:doi/10.1136/jmedgenet-2017-104919; uri/info:scp/85042867516; https://dipot.ulb.ac.be/dspace/bitstream/2013/269534/1/doi_253161.pdfTest; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/269534Test
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3دورية أكاديمية
المؤلفون: Azzi, Salah, Blaise, Annick, Steunou, Virginie, Brioude, Frédéric, Rossignol, Sylvie, Habib, Walid Abi, Bouc, Yves Le, Netchine, Irène, Thibaud, Nathalie, Neves, Cristina Das, Jule, Marilyne Le, Harbison, Madeleine M.D., Salem, Jennifer, Brachet, Cécile, Heinrichs, Claudine
المصدر: Human mutation, 35 (10
مصطلحات موضوعية: Génétique clinique, Biologie, 11p15 region, Fetal and postnatal development, Mutlilocus imprinting disorders, Russell-Silver Syndrome
وصف الملف: 1 full-text file(s): application/pdf
العلاقة: uri/info:doi/10.1002/humu.22623; uri/info:scp/84908693428; https://dipot.ulb.ac.be/dspace/bitstream/2013/187689/3/187689.pdfTest; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/187689Test