TY  - GEN
AU  - Passos-Bueno,Maria Rita
AU  - Armelin,Lucia Maria
AU  - Alonso,Luís Garcia
AU  - Neustein,Isaac
AU  - Sertié,Andréa L
AU  - Abe,Kikue
AU  - Pavanello,Rita de Cássia
AU  - Elkis,Lívia C
AU  - Koiffmann,Célia P
TI  - Craniosynostosis associated with ocular and distal limb defects is very likely caused by mutations in a gene different from FGFR, TWIST, and MSX2
SN  - 0148-7299
PY  - 2003///0407
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Craniosynostoses
KW  - complications
KW  - DNA
KW  - chemistry
KW  - DNA Mutational Analysis
KW  - DNA-Binding Proteins
KW  - genetics
KW  - Exons
KW  - Eye Diseases
KW  - Family Health
KW  - Genetic Predisposition to Disease
KW  - Homeodomain Proteins
KW  - Humans
KW  - Limb Deformities, Congenital
KW  - Male
KW  - Mutation
KW  - Nuclear Proteins
KW  - Protein-Tyrosine Kinases
KW  - Receptor Protein-Tyrosine Kinases
KW  - Receptor, Fibroblast Growth Factor, Type 1
KW  - Receptor, Fibroblast Growth Factor, Type 2
KW  - Receptor, Fibroblast Growth Factor, Type 3
KW  - Receptors, Fibroblast Growth Factor
KW  - Transcription Factors
KW  - Twist-Related Protein 1
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.10752
ER  -