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Reduced transcript expression of genes affected by inherited and de novo CNVs in autism. [electronic resource] by
- Nord, Alex S
- Roeb, Wendy
- Dickel, Diane E
- Walsh, Tom
- Kusenda, Mary
- O'Connor, Kristen Lewis
- Malhotra, Dheeraj
- McCarthy, Shane E
- Stray, Sunday M
- Taylor, Susan M
- Sebat, Jonathan
- King, Bryan
- King, Mary-Claire
- McClellan, Jon M
Producer: 20110913
In:
European journal of human genetics : EJHG vol. 19
Availability: No items available.
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Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome. [electronic resource] by
- Raux, Grégory
- Bumsel, Emilie
- Hecketsweiler, Bernadette
- van Amelsvoort, Therese
- Zinkstok, Janneke
- Manouvrier-Hanu, Sylvie
- Fantini, Carole
- Brévière, Georges-Marie M
- Di Rosa, Gabriella
- Pustorino, Giuseppina
- Vogels, Annick
- Swillen, Ann
- Legallic, Solenn
- Bou, Jacqueline
- Opolczynski, Gaelle
- Drouin-Garraud, Valérie
- Lemarchand, Marie
- Philip, Nicole
- Gérard-Desplanches, Aude
- Carlier, Michèle
- Philippe, Anne
- Nolen, Marie Christine
- Heron, Delphine
- Sarda, Pierre
- Lacombe, Didier
- Coizet, Cyril
- Alembik, Yves
- Layet, Valérie
- Afenjar, Alexandra
- Hannequin, Didier
- Demily, Caroline
- Petit, Michel
- Thibaut, Florence
- Frebourg, Thierry
- Campion, Dominique
Producer: 20070403
In:
Human molecular genetics vol. 16
Availability: No items available.
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295.
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The 22q11 PRODH/DGCR6 deletion is frequent in hyperprolinemic subjects but is not a strong risk factor for ASD. [electronic resource] by
- Richard, Anne Claire
- Rovelet-Lecrux, Anne
- Delaby, Elsa
- Charbonnier, Camille
- Thiruvahindrapuram, Bhooma
- Hatchwell, Eli
- Eis, Peggy S
- Afenjar, Alexandra
- Gilbert Dussardier, Brigitte
- Scherer, Stephen W
- Betancur, Catalina
- Campion, Dominique
Producer: 20161213
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 171B
Availability: No items available.
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300.
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