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Fig. 3 | BMC Medical Genomics

Fig. 3

From: Novel deletion of exon 3 in TYR gene causing Oculocutaneous albinism 1B in an Indian family along with intellectual disability associated with chromosomal copy number variations

Fig. 3

Array- CGH karyogram showing: a, b Deletion of chromosomal region 10q23.2q23.31 in first child and father (Left to right) c Denovo duplication of chromosomal region 13q31.1q31.3 in the third child (male) d–g Deletion of chromosomal region 15q11.1q11.2 in first, the second and third child and father (Left to right)

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BMC Medical Genomics

ISSN: 1755-8794

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