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24. [Phenotypic and genotypic analysis of a fetus carrying an intermediate 22q11.2 deletion encompassing the CRKL gene]. Lin S; Zheng X; Gu H; Li M Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):393-397. PubMed ID: 28604963 [TBL] [Abstract][Full Text] [Related]
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34. Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments. Paylor R; McIlwain KL; McAninch R; Nellis A; Yuva-Paylor LA; Baldini A; Lindsay EA Hum Mol Genet; 2001 Nov; 10(23):2645-50. PubMed ID: 11726551 [TBL] [Abstract][Full Text] [Related]
35. 22q11 deletion syndrome: is that what they used to call . . . ? Umlauf MG Perspect Psychiatr Care; 2008 Oct; 44(4):259-66. PubMed ID: 18826464 [TBL] [Abstract][Full Text] [Related]
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