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Fig. 1 | BMC Medical Genomics

Fig. 1

From: Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case report

Fig. 1

The upper part shows the pedigree of a three-generation Iranian family with two females affected with BWS (black circles). Balanced translocation carriers are represented by a dot in the middle of the symbol. The photographs below show the two-year old girl III.1 and the 36-year-old woman II.7, exhibiting macroglossia and typical facial appearance of BWS

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BMC Medical Genomics

ISSN: 1755-8794

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