Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication–deletion: Genotype–phenotype correlation for anomalies of the corpus callosum
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C. Garel | J. Andrieux | B. Delobel | Marie-Christine Nouguès | M. Gérard | S. Chantot-Bastaraud | J. Siffroi | J. Puechberty | M. Portnoï | C. Coutton | C. Vincent‐Delorme | M. Rio | M. Doco‐Fenzy | D. Heron | N. Chatron | C. Mignot | O. Boute | B. Keren | D. Sanlaville | A. Faudet | M. Rossi | M. Moutard | S. Sigaudy | B. Doray | F. Devillard | V. Malan | C. Pébrel-Richard | S. Whalen | D. Haye | T. Busa | C. Colson | C. Missirian | S. Heide | Roseline Vibert