Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Carole, Goumy"'
Autor:
Carole Goumy, Zangbéwendé Guy Ouedraogo, Elodie Bellemonte, Eleonore Eymard-Pierre, Gwendoline Soler, Isabelle Perthus, Céline Pebrel-Richard, Laetitia Gouas, Gaëlle Salaun, Lauren Véronèse, Hélène Laurichesse, Claude Darcha, Andrei Tchirkov
Publikováno v:
Diagnostics, Vol 13, Iss 23, p 3576 (2023)
Optical genome mapping (OGM) is an alternative to classical cytogenetic techniques to improve the detection rate of clinically significant genomic abnormalities. The isolation of high-molecular-weight (HMW) DNA is critical for a successful OGM analys
Externí odkaz:
https://doaj.org/article/1f9051c7cfc94d40ab7e9c4e7b697bb5
Autor:
Cécile Courdier, John Boudjarane, Valérie Malan, Christine Muti, Brian Sperelakis‐Beedham, Sylvie Odent, Sylvie Jaillard, Chloé Quelin, Cédric Le Caignec, Olivier Patat, Charlotte Dubucs, Sophie Julia, Caroline Schluth‐Bolard, Carole Goumy, Sylvia Redon, Jean‐Baptiste Gaillard, Minh Tuan Huynh, Céline Dupont, Anne‐Claude Tabet, Guillaume Cogan, François Vialard, Rodolphe Dard, Guillaume Jedraszak, Florence Jobic, Mathilde Lefebvre, Geneviève Quenum, Saori Inai, Mélanie Rama, Fanny Sauvestre, Frédéric Coatleven, Julie Thomas, Caroline Rooryck
Publikováno v:
Prenatal Diagnosis
Prenatal Diagnosis, 2023, ⟨10.1002/pd.6340⟩
Prenatal Diagnosis, 2023, ⟨10.1002/pd.6340⟩
International audience; Objective: We aimed to gather fetal cases carrying a 7q11.23 copy number variation (CNV) and collect precise clinical data to broaden knowledge of antenatal features in these syndromes.Methods: We retrospectively recruited unr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2298cfc427024007f848f111933c8ba8
https://hal-u-picardie.archives-ouvertes.fr/hal-04032330
https://hal-u-picardie.archives-ouvertes.fr/hal-04032330
Autor:
Stephan Kemeny, Florence Brugnon, Eléonore Eymard-Pierre, Carole Goumy, Laurent Janny, Andreï Tchirkov, Christine Francannet, Philippe Vago, Céline Pebrel-Richard
Publikováno v:
Asian Journal of Andrology, Vol 19, Iss 1, Pp 135-137 (2017)
Externí odkaz:
https://doaj.org/article/847bb0d9f0c94a2ab5bf441535e82510
Autor:
Gwendoline Soler, Zangbéwendé Guy Ouedraogo, Carole Goumy, Benjamin Lebecque, Gaspar Aspas Requena, Aurélie Ravinet, Justyna Kanold, Lauren Véronèse, Andrei Tchirkov
Publikováno v:
Cancers; Volume 15; Issue 7; Pages: 2131
Cytogenetic aberrations are found in 65% of adults and 75% of children with acute leukemia. Specific aberrations are used as markers for the prognostic stratification of patients. The current standard cytogenetic procedure for acute leukemias is kary
Autor:
Carole Goumy, Lauren Veronese, Rodrigue Stamm, Quentin Domas, Kamil Hadjab, Denis Gallot, Hélène Laurichesse, Amélie Delabaere, Laetitia Gouas, Gaelle Salaun, Céline Perbel-Richard, Philippe Vago, Andrei Tchirkov
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2022, ⟨10.1093/hmg/ddac054⟩
Human Molecular Genetics, 2022, 31 (16), pp.2669-2677. ⟨10.1093/hmg/ddac054⟩
Human Molecular Genetics, Oxford University Press (OUP), 2022, ⟨10.1093/hmg/ddac054⟩
Human Molecular Genetics, 2022, 31 (16), pp.2669-2677. ⟨10.1093/hmg/ddac054⟩
Telomeres protect chromosome ends and control cell division and senescence. During organogenesis, telomeres need to be long enough to ensure the cell proliferation necessary at this stage of development. Previous studies have shown that telomere shor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad4f8fc3225efeac5696f678b1b712b7
https://hal.uca.fr/hal-03737680
https://hal.uca.fr/hal-03737680
Publikováno v:
Morphologie. 106:S18-S19
Autor:
Laetitia Gouas, Nooshin Omar, Gaëlle Salaun, Sophie Besse, Eléonore Eymard-Pierre, Céline Pebrel-Richard, Carole Goumy, Philippe Vago
Publikováno v:
Morphologie. 106:S10-S11
Autor:
Marion Lesieur‐Sebellin, Marianne Till, Philippe Khau Van Kien, Bérénice Herve, Nicolas Bourgon, Céline Dupont, Anne‐Claude Tabet, Mathilde Barrois, Aurélie Coussement, Laurence Loeuillet, Eve Mousty, Vuthy Ea, Amal Assal, Laura Mary, Sylvie Jaillard, Claire Beneteau, Claudine Le Vaillant, Charles Coutton, Françoise Devillard, Carole Goumy, Amélie Delabaere, Sylvia Redon, Yves Laurent, Audrey Lamouroux, Jérôme Massardier, Catherine Turleau, Damien Sanlaville, Vincent Cantagrel, Pascale Sonigo, François Vialard, Laurent J. Salomon, Valérie Malan
Publikováno v:
Prenatal Diagnosis
Prenatal Diagnosis, Wiley, 2021, ⟨10.1002/pd.6074⟩
Prenatal Diagnosis, 2022, 42 (1), pp.118-135. ⟨10.1002/pd.6074⟩
Prenatal Diagnosis, Wiley, 2021, ⟨10.1002/pd.6074⟩
Prenatal Diagnosis, 2022, 42 (1), pp.118-135. ⟨10.1002/pd.6074⟩
International audience; OBJECTIVE: Terminal 6q deletion is a rare genetic condition associated with a neurodevelopmental disorder characterized by intellectual disability and structural brain anomalies. Interestingly, a similar phenotype is observed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c98e980d6de9a1cdbdb7f9b415b26f5
https://hal.archives-ouvertes.fr/hal-03481652
https://hal.archives-ouvertes.fr/hal-03481652
Autor:
Carole Goumy, Claude Darcha, Hélène Laurichesse, Michaela West, Charles Poncet, Jérome Salse, Delphine Voisin, Gaëlle Salaun, Laetitia Gouas, Céline Pebrel-Richard, Lauren Véronèse, Andrei Tchirkov, Gwendoline Soler, Philippe Vago
Publikováno v:
Morphologie. 106:S8
Autor:
Gaëlle Salaun, Eloïse Rodde, Fanny Laffargue, Eléonore Pierre, Carole Goumy, Laetitia Gouas, Christine Francannet, Philippe Vago, Céline Pebrel-Richard
Publikováno v:
Morphologie. 106:S18