Fig. 1From: 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 variationsMLPA results showing TYR exon 3 deletion: (a) All 3 children of fourth-generation with probe ratio 0.00 (b) Carrier parents (Mother with probe ratio 0.47& father with probe ratio 0.49)Back to article page