• A case of dextrocardia, radial ray malformation and renal anomaly
• A new recessive syndrome with VATER-like defects, pulmonary hypertension, abnormal ears, blue sclera, laryngeal webs, and persistent growth deficiency
• A novel germline mutation of the PTEN gene in a patient with macrocephaly, ventricular dilatation, and features of VATER association
• A vascular anomaly of the iliac artery in a patient with VATER association
• Aberrant Right Subclavian Artery-Esophageal Fistula in 20-Year-Old with VATER Association
• Abnormal branching and regression of the notochord and its relationship to foregut abnormalities
• Adults with VATER association: long-term prognosis
• An auricle prosthesis for a boy with the Vater association
• Analysis of cardiac anomalies in VACTERL association
• Analysis of renal anomalies in VACTERL association
• Anorectal Malformations and Late-Term Problems
• Another observation with VATER association and a complex IV respiratory chain deficiency
• Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations
• Asymmetric osteotomy of the spine for coronal imbalance: a technical report
• Carpal tunnel syndrome in children. About 10 clinical cases
• Caudal duplication syndrome with unilateral hypoplasia of the pelvis and lower limb and ventriculoseptal heart defect in a mother and features of VATER association in her child
• Caudal regression and tracheoesophageal malformation induced by adriamycin: a novel chick model of VATER association
• Clinical geneticists' views of VACTERL/VATER association
• Coats disease and VATER association in a 5-year-old boy
• Combined operation for congenital cardiovascular and other anomalies in children
• Congenital absence of the long head of the biceps brachii tendon as a VATER association
• Congenital blepharoptosis co-occurring with VATER association
• Cystic dysplasia of the rete testis in an adolescent with VATER association
• De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL-like association and analysis of EFNB2 in patients with anorectal malformations
• De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association
• Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype?
• Evidence for annular pancreas as an associated anomaly in the VATER/VACTERL association and investigation of the gene encoding pancreas specific transcription factor 1A as a candidate gene
• Evidence for inheritance in patients with VACTERL association
• Expanding the phenotypic spectrum of the Baller-Gerold syndrome
• Familial occurrence of the VATER/VACTERL association
• First Trimester Diagnosis of VACTERL Association
• Genetic analysis of anal atresia in pigs: evidence for segregation at two main loci
• Genetic Disruption of Cilia-Associated Signaling Pathways in Patients with VACTERL Association
• Gross hematuria in the VATER association: coincidence or association
• Hedgehog in the human: a possible explanation for the VATER association
• Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies
• Higher incidence of thyroid agenesis in Mexican newborns with congenital hypothyroidism associated with birth defects
• Histologic characterization of the major duodenal papilla and association with concurrent biliary, pancreatic, and intestinal pathology in cats
• HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum
• Inheritance of the VATER/VACTERL association
• Is urorectal septum malformation sequence a variant of the vertebral defects, anal atresia, tracheo-oesophageal fistula, renal defects and radial dysplasia association? Report of a case and a review of the literature
• KL-6 mucin expression in carcinoma of the ampulla of Vater: association with cancer progression
• Laryngo-tracheo-oesophageal clefts
• Lethal comorbidity with genital anomaly in the infant
• Maternal asthma medication use and the risk of selected birth defects
• Mechanisms for the development of esophageal atresia
• Medical predictors of psychological anxieties in VATER patients
• Mitochondrial Factors and VACTERL Association-Related Congenital Malformations
• Monochorionic-monoamniotic twins discordant for VATER association
• Müllerian anomaly in a woman with Hirschsprung's disease
• Multidisciplinary approach to paediatric aerodigestive disorders: A single-centre longitudinal observational study
• Mutations in PTF1A are not a common cause for human VATER/VACTERL association or neural tube defects mirroring Danforth's short tail mouse
• Nonfamilial VACTERL-H Syndrome in a Dizygotic Twin: Prenatal Ultrasound and Postnatal 3D CT Findings
• Normal exon copy number of the GLI2 and GLI3 genes in patients with esophageal atresia
• Oesophageal atresia with tracheoesophageal fistula and anal atresia in a patient with a de novo microduplication in 17q12
• Ontogeny of the VATER kidney in a rat model
• Partial urorectal septum malformation sequence: a report of 25 cases
• Pediatric renal transplantation and the dysfunctional bladder
• Phenotypic diversity of patients diagnosed with VACTERL association
• Prenatal diagnosis of a case with anencephaly-omphalocele-unilateral absent radial ray
• Prenatal diagnosis of apparently isolated unilateral multicystic kidney: implications for counselling and management
• Prenatal diagnosis of distal 13q deletion syndrome in a fetus with esophageal atresia: a case report and review of the literature
• Prenatal diagnosis of persistent cloaca associated with VATER (vertebral defects, anal atresia, tracheo-esophageal fistula, and renal dysplasia)
• Prognostic impact of postoperative infection after resection of biliary malignancy: A multicenter retrospective cohort study
• Progressive congenital torticollis in VATER association syndrome
• Renal anomalies in the VATER animal model
• Renal transplantation in Vater association patient: case report
• Renovascular hypertension complicated with VATER association
• Second study on the recurrence risk of isolated esophageal atresia with or without trachea-esophageal fistula among first-degree relatives: no evidence for increased risk of recurrence of EA/TEF or for malformations of the VATER/VACTERL association spectr
• Serial Hunt for Ciliary Genes in Complex Syndromes
• Sirenomelia with esophageal atresia
• Sirenomelia: case reports and current concepts of pathogenesis
• Somatic mosaicism in esophageal atresia
• Supernumerary kidney in a term infant with VATER association
• Switched-on Sonic hedgehog: a gene whose activity extends beyond fetal development--to oncogenesis
• Sympathetic ophthalmia in vater association combined with persisting hyperplastic primary vitreous after cyclodestructive procedure
• Sympathetic ophthalmia in vater association combined with persisting hyperplastic primary vitreous after cyclodestructive procedure
• Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association
• The etiology of VACTERL association: Current knowledge and hypotheses
• The illusion of severe carpal tunnel syndrome (CTS)
• Three novel mutations of the PAX6 gene in Japanese aniridia patients
• Tracheal agenesis, a frightening scenario
• Tracheoesophageal fistula (H-type) in neonates with imperforate anus and the VATER association
• Triple Atresia, Triple Threat? An Unusual Constellation of Primary Surgical Abnormalities
• Tumor necrosis factor-alpha inhibition and VATER association: a causal relationship
• Underlying genetic factors of the VATER/VACTERL association with special emphasis on the "Renal" phenotype
• Urethral duplication in a child with VATER association
• Urinary reconstruction in vertebral, anorectal, cardiac, trachea-esophageal, renal abnormalities and limb defects association with chronic renal failure and penile duplication
• Urogenital sinus, rectovaginal fistula, and an anterior stenosed anus--another cloacal variant
• Urological anomalies in anorectal malformations in The Netherlands: effects of screening all patients on long-term outcome
• VACTERL Association Complicated with Right-sided Congenital Diaphragmatic Hernia
• VACTERL Association in a Female Pig (Sus scrofa domesticus)
• VACTERL-H Association and Fanconi Anemia
• VACTERL/VATER Association
• VATER association
• VATER Association
• VATER association with multiple ribs anomalies
• VATER/VACTERL Association and Caudal Regression with Xq25-q27.3 Microdeletion: A Case Report
• VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis
• Vestibular Derangement and Motion Intolerance in VATER Association