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Fig. 1 | Clinical Epigenetics

Fig. 1

From: Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances

Fig. 1

Pedigrees of families 2–10. Black filled symbol represents the probands affected by BWS or PHP1B, black central dots the unaffected carrier mothers. Triangles: spontaneous miscarriage. Triangle with line: voluntary termination of pregnancy. The variants in bold are rare (AF < 0.01), those in regular font style are common (AF > 0.01). The asterisks indicate the family members whose DNA was not available for genetic analyses

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