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Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2011, Volume 6, Issue 1, pp. 56 - 56
VACTERL/VATER association is typically defined by the presence of at least three of the following congenital malformations: vertebral defects, anal atresia,... 
RESPIRATORY-CHAIN DEFICIENCY | MEDICINE, RESEARCH & EXPERIMENTAL | MULTIPLE CONGENITAL-ANOMALIES | GENOTYPE-PHENOTYPE CORRELATIONS | PRENATAL SONOGRAPHIC DIAGNOSIS | VATER-ASSOCIATION | TOWNES-BROCKS-SYNDROME | ACID RECEPTORS RARS | GENETICS & HEREDITY | PALLISTER-HALL-SYNDROME | RIGHT PULMONARY AGENESIS | HOLT-ORAM-SYNDROME | Abnormalities, Multiple - pathology | Limb Deformities, Congenital - genetics | Radius - pathology | Kidney - pathology | Humans | Male | Tracheoesophageal Fistula - complications | Anus, Imperforate - pathology | Spine - abnormalities | Heart Defects, Congenital - genetics | Abnormalities, Multiple - epidemiology | Female | Spine - pathology | Anal Canal - pathology | Abnormalities, Multiple - genetics | Anus, Imperforate - diagnosis | Infant, Newborn | Trachea - abnormalities | Tracheoesophageal Fistula - epidemiology | Anus, Imperforate - complications | Heart Defects, Congenital - pathology | Radius - abnormalities | Esophagus - abnormalities | Anal Canal - abnormalities | Trachea - pathology | Limb Deformities, Congenital - diagnosis | Esophagus - pathology | Heart Defects, Congenital - complications | Kidney - abnormalities | Limb Deformities, Congenital - epidemiology | Abnormalities, Multiple - diagnosis | Anus, Imperforate - genetics | Tracheoesophageal Fistula - genetics | Heart Defects, Congenital - epidemiology | Heart Defects, Congenital - diagnosis | Limb Deformities, Congenital - complications | Anus, Imperforate - epidemiology | Limb Deformities, Congenital - pathology | Care and treatment | Genetic aspects | Prognosis | Diagnosis | VATER syndrome
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2010, Volume 86, Issue 3, pp. 434 - 439
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 5/2009, Volume 106, Issue 21, pp. 8573 - 8578
Journal Article
Journal Article
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 01/2011, Volume 20, Issue 2, pp. 271 - 285
Brachydactyly type B (BDB1) and Robinow syndrome (RRS) are two skeletal disorders caused by mutations in ROR2, a co-receptor of Wnt5a. Wnt5a/Ror2 can activate... 
PLANAR-CELL-POLARITY | APICAL ECTODERMAL RIDGE | ZEBRAFISH GASTRULATION | WNT/BETA-CATENIN | NEURAL-TUBE DEFECTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | CANONICAL WNT PATHWAY | CONVERGENT EXTENSION | BETA-CATENIN | RECEPTOR TYROSINE KINASE | FEEDBACK LOOP | Abnormalities, Multiple - pathology | Limb Deformities, Congenital - genetics | Maxillofacial Abnormalities - genetics | Bone Morphogenetic Protein 4 - genetics | Bone Morphogenetic Protein 4 - antagonists & inhibitors | Cell Survival - genetics | Limb Deformities, Congenital - embryology | Wnt-5a Protein | Wnt Proteins - metabolism | Spine - abnormalities | Intercellular Signaling Peptides and Proteins - metabolism | Musculoskeletal Development - genetics | Wnt Proteins - genetics | Limb Buds - abnormalities | Spine - embryology | Spine - pathology | Abnormalities, Multiple - genetics | Maxillofacial Abnormalities - embryology | Morphogenesis - genetics | Receptor Tyrosine Kinase-like Orphan Receptors - metabolism | Limb Deformities, Congenital - metabolism | Gene Dosage | Signal Transduction - genetics | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Maxillofacial Abnormalities - pathology | Animals | Cell Polarity - physiology | Receptor Tyrosine Kinase-like Orphan Receptors - genetics | Mice | Mutation | Limb Deformities, Congenital - pathology
Journal Article