TY  - GEN
AU  - Twigg,Stephen R F
AU  - Versnel,Sarah L
AU  - Nürnberg,Gudrun
AU  - Lees,Melissa M
AU  - Bhat,Meenakshi
AU  - Hammond,Peter
AU  - Hennekam,Raoul C M
AU  - Hoogeboom,A Jeannette M
AU  - Hurst,Jane A
AU  - Johnson,David
AU  - Robinson,Alexis A
AU  - Scambler,Peter J
AU  - Gerrelli,Dianne
AU  - Nürnberg,Peter
AU  - Mathijssen,Irene M J
AU  - Wilkie,Andrew O M
TI  - Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene
SN  - 1537-6605
PY  - 2009///0609
KW  - Child
KW  - Chromosomes, Human, Pair 1
KW  - genetics
KW  - Craniofacial Abnormalities
KW  - Homeodomain Proteins
KW  - Humans
KW  - Infant, Newborn
KW  - Mutation
KW  - Nasal Bone
KW  - abnormalities
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.ajhg.2009.04.009
ER  -