Char syndrome is an autosomal dominant congenital disease caused by mutations in TFAP2B gene which affects the development of the bones of the face as...

Cri du chat syndrome is a rare genetic disorder due to a partial chromosome deletion on chromosome 5. Its name is a French term ("cat-cry" or "call of...

in association with many syndromes and other conditions: McKusick–Kaufman syndrome Char syndrome Simpson–Golabi–Behmel syndrome A possible connection with...

distinct syndrome from an allelic variant of Char syndrome. Hand anomalies include metacarpal hypoplasia. It is unknown if heart-hand syndromes are caused...

Chandler's syndrome Chands syndrome Chang–Davidson–Carlson syndrome Chaotic atrial tachycardia Char syndrome Charcot d Charcot disease Charcot–Marie–Tooth disease...

(Concept Id: C1854108)". www.ncbi.nlm.nih.gov. Retrieved 2023-07-02. "Char syndrome (Concept Id: C1868570)". www.ncbi.nlm.nih.gov. Retrieved 2023-07-05...

Liu Q, Qiu J, Ding X. KCTD1 mutants in scalp ear nipple syndrome and AP 2α P59A in Char syndrome reciprocally abrogate their interactions, but can regulate...

and repressor. Mutations in this gene result in autosomal dominant Char syndrome, suggesting that this gene functions in the differentiation of neural...

Cervical cancer, somatic; 603956; FGFR3 Chanarin–Dorfman syndrome; 275630; ABHD5 Char syndrome; 169100; TFAP2B Charcot–Marie–Tooth disease, axonal, type...

Tribute to an Artist 1979 52nd 1 1 The Tin Drum 1979 52nd 1 1 The China Syndrome 1979 52nd 0 4 The Rose 1979 52nd 0 4 1941 1979 52nd 0 3 La Cage aux Folles...