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	1.	A founder nonsense variant in NUDT2 causes a recessive neurodevelopmental disorder in Saudi Arab children. [electronic resource] by Yavuz, H Bertoli-Avella, A M Alfadhel, M Al-Sannaa, N Kandaswamy, K K Al-Tuwaijri, W Rolfs, A Brandau, O Bauer, P Producer: 20191028 In: Clinical genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Expanding the clinical and genetic spectra of NKX6-2-related disorder. [electronic resource] by Baldi, C Bertoli-Avella, A M Al-Sannaa, N Alfadhel, M Al-Thihli, K Alameer, S Elmonairy, A A Al Shamsi, A M Abdelrahman, H A Al-Gazali, L Shawli, A Al-Hakami, F Yavuz, H Kandaswamy, K K Rolfs, A Brandau, O Bauer, P Producer: 20190925 In: Clinical genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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