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Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: Exome sequencing for diagnosis of congenital hemolytic anemia

Fig. 2

Pedigrees of 3 HS families and 6 UH families. Legend: Black squares: affected males; black circles: affected females; open squares: unaffected males; open circles: unaffected females; arrow: the proband. 2a = P11 family pedigree (HS); 2b = P10 family pedigree (HS); 2c = P4 family pedigree (HS); 2d = P25 family pedigree (CDA2); 2e = P27 family pedigree (UH); 2f: P31 family pedigree (GARDOS); 2 g: P33 family pedigree (UH); 2 h: P36 family pedigree (multiple association); 2i: P40 family pedigree (ATP11C hemolysis)

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