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Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU. [electronic resource] by
- Depienne, Christel
- Nava, Caroline
- Keren, Boris
- Heide, Solveig
- Rastetter, Agnès
- Passemard, Sandrine
- Chantot-Bastaraud, Sandra
- Moutard, Marie-Laure
- Agrawal, Pankaj B
- VanNoy, Grace
- Stoler, Joan M
- Amor, David J
- Billette de Villemeur, Thierry
- Doummar, Diane
- Alby, Caroline
- Cormier-Daire, Valérie
- Garel, Catherine
- Marzin, Pauline
- Scheidecker, Sophie
- de Saint-Martin, Anne
- Hirsch, Edouard
- Korff, Christian
- Bottani, Armand
- Faivre, Laurence
- Verloes, Alain
- Orzechowski, Christine
- Burglen, Lydie
- Leheup, Bruno
- Roume, Joelle
- Andrieux, Joris
- Sheth, Frenny
- Datar, Chaitanya
- Parker, Michael J
- Pasquier, Laurent
- Odent, Sylvie
- Naudion, Sophie
- Delrue, Marie-Ange
- Le Caignec, Cédric
- Vincent, Marie
- Isidor, Bertrand
- Renaldo, Florence
- Stewart, Fiona
- Toutain, Annick
- Koehler, Udo
- Häckl, Birgit
- von Stülpnagel, Celina
- Kluger, Gerhard
- Møller, Rikke S
- Pal, Deb
- Jonson, Tord
- Soller, Maria
- Verbeek, Nienke E
- van Haelst, Mieke M
- de Kovel, Carolien
- Koeleman, Bobby
- Monroe, Glen
- van Haaften, Gijs
- Attié-Bitach, Tania
- Boutaud, Lucile
- Héron, Delphine
- Mignot, Cyril
Producer: 20170620
In:
Human genetics vol. 136
Availability: No items available.
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