Genetics of EA-TEF Crossword

Rarα and Rarβ
Pathway effectors Shh, Gli2, Gli3, Foxf1
Transcription factors Hoxc4, Ttf-1, Pcsk5
22q11.2 deletion syndrome. Also associated with congenital heart problems, specific facial features, frequent infections, developmental delay, learning problems and cleft palate.
Trisomy 13, 18, 21
oculo-genito-laryngeal syndrome (7-dehydrocholesterol reductase deficiency)
Syndrome with MYCN single-gene mutation
Syndrome with CHD7 single-gene mutation (coloboma, heart defects, atresia choanae, developmental retardation, genital hypoplasia, and ear deformities)
SOX2 single-gene mutation
Syndrome with GL13 single-gene mutation
FANCA single-gene mutation
oculo-auriculo-vertebral syndrome
Syndrome associated with pancreatic hypoplasia, intestinal atresia, gall bladder hypoplasia
Syndrome with bilateral renal agenesis
atrio-digital syndrome
congenital syndrome of facial abnormalities
Sequence associated with congenital cardiac malformations, splenic dysgenesis, symmetric development of normally asymmetric organs