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The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients.
Leroy, Camille; Landais, Emilie; Briault, Sylvain; David, Albert; Tassy, Olivier; Gruchy, Nicolas; Delobel, Bruno; Grégoire, Marie-José; Leheup, Bruno; Taine, Laurence; Lacombe, Didier; Delrue, Marie-Ange; Toutain, Annick; Paubel, Agathe; Mugneret, Francine; Thauvin-Robinet, Christel; Arpin, Stéphanie; Le Caignec, Cedric; Jonveaux, Philippe; Beri, Mylène; Leporrier, Nathalie; Motte, Jacques; Fiquet, Caroline; Brichet, Olivier; Mozelle-Nivoix, Monique; Sabouraud, Pascal; Golovkine, Nathalie; Bednarek, Nathalie; Gaillard, Dominique; Doco-Fenzy, Martine.
Affiliation
  • Leroy C; CHU-Reims, HMB, Service de génétique, Reims, France.
Eur J Hum Genet ; 21(6): 602-12, 2013 Jun.
Article in En | MEDLINE | ID: mdl-23073310
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Behavior / Chromosome Disorders / Overweight / Brachydactyly / Fibrous Dysplasia, Polyostotic / Intellectual Disability Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: Eur J Hum Genet Year: 2013 Document type: Article
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Behavior / Chromosome Disorders / Overweight / Brachydactyly / Fibrous Dysplasia, Polyostotic / Intellectual Disability Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: Eur J Hum Genet Year: 2013 Document type: Article