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Fig. 3 | BMC Medical Genetics

Fig. 3

From: Exome sequencing identified rare variants in genes HSPG2 and ATP2B4 in a family segregating developmental dysplasia of the hip

Fig. 3

Sequence chromatograms of heterozygous variants identified in all three individuals of a family segregating DDH. The upper panel (a) represents the nucleotide sequences in all affected individuals in HSPG2 (c.3328G > T) gene and the lower panel (c) represents the nucleotide sequences in all affected individuals in ATP2B4 (c.2264G > A) gene. Panel b and d shows partial nucleotide sequence of the control individuals for HSPG2 and ATP2B4. Arrow head indicates the variant site

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BMC Medical Genetics

ISSN: 1471-2350

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