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1 Ergebnisse
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Neurodevelopmental phenotype in 36 new patients with 8p inv..:
Vibert, Roseline
;
Mignot, Cyril
;
Keren, Boris
...
Clinical Genetics. 101 (2021) 3 - p. 307-316 , 2021
Link:
https://doi.org/10.1111/cge.14096
RT Journal T1
Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication–deletion: Genotype–phenotype correlation for anomalies of the corpus callosum
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.14096&Exemplar=1&LAN=DE A1 Vibert, Roseline A1 Mignot, Cyril A1 Keren, Boris A1 Chantot‐Bastaraud, Sandra A1 Portnoï, Marie‐France A1 Nouguès, Marie‐Christine A1 Moutard, Marie‐Laure A1 Faudet, Anne A1 Whalen, Sandra A1 Haye, Damien A1 Garel, Catherine A1 Chatron, Nicolas A1 Rossi, Massimiliano A1 Vincent‐Delorme, Catherine A1 Boute, Odile A1 Delobel, Bruno A1 Andrieux, Joris A1 Devillard, Françoise A1 Coutton, Charles A1 Puechberty, Jacques A1 Pebrel‐Richard, Céline A1 Colson, Cindy A1 Gerard, Marion A1 Missirian, Chantal A1 Sigaudy, Sabine A1 Busa, Tiffany A1 Doco‐Fenzy, Martine A1 Malan, Valérie A1 Rio, Marlène A1 Doray, Bérénice PB Wiley YR 2021 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 101 IS 3 SP 307 OP 316 LK http://dx.doi.org/https://doi.org/10.1111/cge.14096 DO https://doi.org/10.1111/cge.14096 SF ELIB - SuUB Bremen
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