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TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons
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Recessive LAMC3 mutations cause malformations of occipital cortical development
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Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
S Yilmaz, N Koçer, B Tüysüz, K Yasuno, M Choi, M Topçu, H Kaymakçalan, AK Öztürk, A Louvi, B Tatli, MN Pamir, RA Bronen, A Dinçer, C Yalçinkaya, MH Johnson, M Bakircioǧlu, N Šestan, M Özmen, W Ho, D Yalnizoǧlu, S Gökben, RP Lifton, Kenneth Kwan, AO Çaǧlayan, Y Zhu, S Sanders, S Mane, S Kumandaş, MW State, K Bilgüvar, M Günel, T Barak, H Per
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