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Fig. 1 | BMC Medical Genomics

Fig. 1

From: A novel 268 kb deletion combined with a splicing variant in IL7R causes of severe combined immunodeficiency in a Chinese family: a case report

Fig. 1

A Chinese family presents severe combined immunodeficiency (SCID). A Bone marrow aspirate smear with features of hemophagocytosis showing neutrophils engulfed by macrophages (Jenner Giemsa, ×400). B Pedigree of the family with SCID. Circles and squares indicate females and males respectively; filled symbols represent affected individuals with SCID; slashed symbols are deceased members; open symbols represent healthy individuals. Black arrow indicates the proband. The proband’s unaffected mother and father are carriers of the splicing variant and deletion respectively. WT, wild-type; ND, not determined

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BMC Medical Genomics

ISSN: 1755-8794

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