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. 2011 May 18;1(5):211–222. doi: 10.1159/000328203

Table 4.

Clinical manifestations of patients with TGIF alterations (including probands and mutation or deletion-positive relatives)

Clinical feature Patients (n = 25) with intragenic TGIF mutations n (%) Patients (n = 18) with TGIF deletions n (%) p valuea
Microcephaly 10 (40) 9(50) 0.5496
Hypotelorism 9(36) 3(17) 0.1911
Cleft lip and/or palate 9(36) 7(39) 0.8994
Midface hypoplasia 8(32) 7(39) 0.7497
Single maxillary central incisor 2(8) 6(33) 0.0517
Hypopituitarism 4(16) 5(28) 0.4554
Extra-neuronal/craniofacial findings 0 6(33) 0.0030*
Total 25 18 N/A
*

Significant; N/A = not applicable.

a

By 2-tailed Fisher's exact test or χ2 when appropriate.