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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Complex translocation disrupting TCF4 and altering TCF4 isoform expression segregates as mild autosomal dominant intellectual disability

Fig. 1

Clinical photographs of the proband (arrow, III-3), his affected father (II-1) and affected paternal grandmother (I-2). (a) Family pedigree. Affected individuals are shown by black symbols. (b, c) Frontal and profile head photographs of the proband at age 2.4 years. (d) Profile head photograph of the proband at age 3.4 years. (e, f) Frontal and profile head photographs of the proband’s father at age 30 years. (g, h) Frontal and profile head photographs of the proband’s paternal grandmother at age 53 years

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172