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Fig. 4 | BMC Medical Genomics

Fig. 4

From: Xp11.22 duplications in four unrelated Chinese families: delineating the genotype-phenotype relationship for HSD17B10 and FGD1

Fig. 4

A genome view of all Xp11.22 duplication cases. The panel shows a genome view of all Xp11.22 duplication cases (blue colored custom tracks) extracted from Human Genome Build 37 (hg19). The minimal overlapping region of one of our probands (Family 1) and DECIPHER 263219 only spans the entire HSD17B10 gene, which is surrounded by a red box. The FGD1 gene is duplicated exclusively in two of our probands (Families 3 and 4) and DECIPHER 249490, which is surrounded by a black box

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BMC Medical Genomics

ISSN: 1755-8794

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