TY  - GEN
AU  - Vasudevan,Pradeep C
AU  - Twigg,Stephen R F
AU  - Mulliken,John B
AU  - Cook,Jackie A
AU  - Quarrell,Oliver W J
AU  - Wilkie,Andrew O M
TI  - Expanding the phenotype of craniofrontonasal syndrome: two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia
SN  - 1018-4813
PY  - 2006///0822
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Child, Preschool
KW  - Craniofacial Abnormalities
KW  - Ephrin-B1
KW  - Female
KW  - Genetic Diseases, X-Linked
KW  - Hernia, Diaphragmatic
KW  - Hernias, Diaphragmatic, Congenital
KW  - Humans
KW  - Infant, Newborn
KW  - Male
KW  - Phenotype
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/sj.ejhg.5201633
ER  -