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Author/Creator Landais, Emilie

1. 1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients. Issue 2 (11th November 2022)

Authors:
Jacquin, Clémence; Landais, Emilie; Poirsier, Céline; Afenjar, Alexandra; Akhavi, Ahmad; Bednarek, Nathalie; Bénech, Caroline; Bonnard, Adeline; Bosquet, Damien; Burglen, Lydie; Callier, Patrick; Chantot‐Bastaraud, Sandra; Coubes, Christine; Coutton, Charles; Delobel, Bruno; Descharmes, Margaux; ...
Journal:
American journal of medical genetics
Issue:
Volume 191:Issue 2(2023)
Page Start:
445
Record Type:
Journal Article
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2. A pure familial 6q15q21 split duplication associated with obesity and transmitted with partial reduction. (21st April 2015)

Authors:
Landais, Emilie; Leroy, Camille; Kleinfinger, Pascale; Brunet, Stéphanie; Koubi, Valérie; Pietrement, Christine; Poli‐Mérol, Marie‐Laurence; Fiquet, Caroline; Souchon, Pierre‐François; Beri, Mylène; Jonveaux, Philippe; Garnotel, Roselyne; Gaillard, Dominique; Doco‐Fenzy, Martine
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 6(2015:Jun.)
Page Start:
1275
Record Type:
Journal Article
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3. Clinical and genomic delineation of the new proximal 19p13.3 microduplication syndrome. Issue 1 (5th October 2022)

Authors:
Jouret, Guillaume; Egloff, Matthieu; Landais, Emilie; Tassy, Olivier; Giuliano, Fabienne; Karmous‐Benailly, Houda; Coutton, Charles; Satre, Véronique; Devillard, Françoise; Dieterich, Klaus; Vieville, Gaëlle; Kuentz, Paul; le Caignec, Cédric; Beneteau, Claire; Isidor, Bertrand; Nizon, Mathilde; C...
Journal:
American journal of medical genetics
Issue:
Volume 191:Issue 1(2023)
Page Start:
52
Record Type:
Journal Article
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4. Microtriplication of 11q24.1: a highly recognisable phenotype with short stature, distinctive facial features, keratoconus, overweight, and intellectual disability. Issue 9 (26th May 2011)

Authors:
Beneteau, Claire; Landais, Emilie; Doco-Fenzy, Martine; Gavazzi, Cyrille; Philippe, Christophe; Béri-Dexheimer, Mylène; Bonnet, Céline; Vigneron, Jacqueline; Walrafen, Pierre; Motte, Jacques; Leheup, Bruno; Jonveaux, Philippe
Journal:
Journal of medical genetics
Issue:
Volume 48:Issue 9(2011)
Page Start:
635
Record Type:
Journal Article
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