Fig. 2: Photographs of affected individuals with associated with variant types. | Genetics in Medicine

Fig. 2: Photographs of affected individuals with associated with variant types.

From: GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder

Fig. 2

a–e Nonsense or truncating frameshift variants: (a) GAND19, (b) GAND18, (c) GAND33 and GAND34, (d) GAND53, ( e) GAND20. f–k Missense variants: (f) GAND28, (g) GAND15, (h) GAND52, (i) GAND32, (j) GAND55, (k) GAND49. l–q Splice-site variants: (l) GAND17, (m) GAND27, (n) GAND42, (o) GAND21, (p) GAND6. q–w Nonsense or truncating frameshift variants: (q) GAND40, (r) GAND12, (s) GAND3, (t) GAND13, (u) GAND8, (v) GAND36, (w) GAND2. Composite of 19 photographs of (x) GAND subjects. and (y) 19 healthy controls (FDNA Inc. USA).

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