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. Author manuscript; available in PMC: 2023 May 1.
Published in final edited form as: Clin Genet. 2022 Apr 12;101(5-6):530–540. doi: 10.1111/cge.14132

Figure 2.

Figure 2.

a: frontal view of Subject 1 (F1-II3) showing: facial asymmetry, bitemporal narrowing, thick and arched eyebrows, upslanted and narrow palpebral fissures, hypertelorism, fullness of upper eyelids, and full cheeks. b: frontal view of Subject 2 (F1-II7) showing: Broad forehead and epicanthal folds. c and d: frontal and lateral views of Subject 4 (F3-II1): long face, bitemporal narrowing, thick and arched eyebrows, downslanted palpebral fissures, large ears, long philtrum, thin upper lip, and broad chin. e and f: frontal and lateral views of Subject 6 (F4-II5) showing narrow palpebral fissures, hypertelorism, large ears, thick lips, long philtrum, and retromicrognathia. g: frontal view of Subject 9 (F5-III11) showingelongated face, bitemporal narrowing, thick and arched eyebrows with synophrys, epicanthal folds, hypertelorism, large ears, depressed nasal bridge, maxillary hypoplasia, long philtrum, and elongated jaw. h: frontal view of Subject 11 (F6-II8) showing elongated face, bitemporal narrowing, thick and arched eyebrows, hypertelorism, large ears, depressed nasal bridge, maxillary hypoplasia, long and smooth philtrum, and elongated jaw.