Results
|
301.
|
|
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302.
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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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303.
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304.
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305.
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306.
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307.
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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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308.
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310.
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311.
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312.
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The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders. [electronic resource] by
- Drew, Liam J
- Crabtree, Gregg W
- Markx, Sander
- Stark, Kimberly L
- Chaverneff, Florence
- Xu, Bin
- Mukai, Jun
- Fenelon, Karine
- Hsu, Pei-Ken
- Gogos, Joseph A
- Karayiorgou, Maria
Producer: 20110720
In:
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience vol. 29
Availability: No items available.
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313.
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318.
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319.
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320.
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Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes. [electronic resource] by
- Zarchi, Omer
- Carmel, Miri
- Avni, Chen
- Attias, Josef
- Frisch, Amos
- Michaelovsky, Elena
- Patya, Miriam
- Green, Tamar
- Weinberger, Ronnie
- Weizman, Abraham
- Gothelf, Doron
Producer: 20140513
In:
Journal of psychiatric research vol. 47
Availability: No items available.
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