• A case of double cystic esophageal duplication in VACTERL syndrome: the first case report and a review of the literature
• A case report of Gollop-Wolfgang complex in 12 years old boy
• A missense variant at the RAC1-PAK1 binding site of RAC1 inactivates downstream signaling in VACTERL association
• A Network of Anomalies Prompting VACTERL Workup in a Trisomy 21 Newborn
• A novel genotype-phenotype between persistent-cloaca-related VACTERL and mutations of 8p23 and 12q23.1
• A Novel VACTERL Assessment Tool to Facilitate Counseling for Expectant Families
• A Population-Based Cohort Study on Diagnosis and Early Management of Anorectal Malformation in the UK and Ireland
• A Uncommon Case: Kasabach-Merritt syndrome with VACTERL Association
• Absent Thumb and Radius in a Neonate With Tracheo-Esophageal Fistula and Ventricular Septal Defect: VACTERL Association
• An unusual presentation of pacifier thumb duplication with VACTERL association: Case report and review of literature
• Analysis of mortality and long-term outcomes of pediatric patients with tracheoesophageal fistula/esophageal atresia
• Anorectal malformations (ARM) and VACTERL association and severity of congenital heart diseases (CHD): Experience of 396 consecutive patients in a tertiary center
• Anorectal Malformations and Late-Term Problems
• Aphallia in a neonate with VACTERL malformation: report of a rare association
• Assisted Reproductive Technology and Anorectal Malformation: A Single-Center Experience
• Associated anomalies in anophthalmia and microphthalmia
• Bacterial Sepsis among Children with Congenital Heart Disease in Tikur Anbessa Specialized Hospital, Addis Ababa, Ethiopia
• Bovine Aortic Arch with an Aberrant Left Vertebral Artery in a 3-Year-Old Boy with VACTERL Association: A Case Report
• Cartilage within lipomyelomeningocele and ulnar longitudinal deficiency syndrome as VACTERL association, alliance in SHH/GLI3, and Wnt pathway: illustrative case
• Cervicothoracic dislocation due to congenital and bone-dysplasia-related vertebral malformations
• Challenges in prenatal diagnosis of foetal anorectal malformation and hydrocolpos - Case report
• Chromosomal abnormalities associated with fetal megacystis
• Clinical and genetic approach in the characterization of newborns with anorectal malformation
• Clinical features of Mayer-Rokitansky-Küster-Haüser syndrome diagnosed at under 16 years old: results from a questionnaire survey conducted on all institutions of pediatric surgery and pediatric urology in Japan
• Clinical Presentations and Diagnostic Imaging of VACTERL Association
• Cloacal Malformation with Associated Urethral Atresia
• COL11A2 as a candidate gene for vertebral malformations and congenital scoliosis
• Combined esophageal and duodenal atresia: A review of the literature from 1950 to 2020
• Congenital Heart Defects in Patients with Anorectal Malformations: A Retrospective Cohort Study of 281 Patients
• Congenital musculoskeletal anomalies - key radiographic findings
• Congenital superior oblique palsy in a patient with VACTERL association
• Delayed finding of congenital duodenal obstruction following congenital diaphragmatic hernia repair
• Does presence of a VACTERL anomaly predict an associated gynecologic anomaly in females with anorectal malformations?: A Pediatric Colorectal and Pelvic Learning Consortium Study
• Ear anomalies and hearing loss in patients with VACTERL association and the effect of maternal diabetes
• Ectopic scrotum and penoscrotal transposition: Case report and literature review
• Endoscopic Ventriculocysternostomy, Magendie Foraminoplasty, and Plexusectomy With Craniovertebral Shunt Placement in a Pediatric Patient With Hydrocephalus and VACTERL Association: A Novel Treatment Option
• Esophageal Atresia
• Esophageal Atresia Associated with Congenital Duodenal Obstruction: Turkish Esophageal Atresia Registry (TEAR) Evaluation
• Esophageal Heterotopic Pancreas in an Asymptomatic 2-Year-Old With VACTERL Association
• Expansion of the core features of VACTERL association to include genital anomalies
• Extra-cardiac diagnoses and postnatal outcomes of fetal tetralogy of fallot
• Fetal Diagnosis of Scimitar Syndrome in the Presence of Complex Congenital Heart Disease
• Fetal Scoliosis: Natural History and Outcomes
• Fetal Tethered Spinal Cord: Diagnostic Features and Its Association with Congenital Anomalies
• Fibrofatty filum terminale: long-term outcomes from a Singapore children's hospital
• Further description of two patients with biallelic variants in NADSYN1 in association with cardiac and vertebral anomalies
• Genetic Disruption of Cilia-Associated Signaling Pathways in Patients with VACTERL Association
• Genetic Evidence for Congenital Vascular Disorders in Patients with VACTERL Association
• Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort
• Gray Platelet Syndrome in a Neonate With VACTERL Association: A Novel Homozygous Pathogenic Variant c.5257C>T in the NBEAL2 Gene
• Gray Platelet Syndrome in a Neonate With VACTERL Association: A Novel Homozygous Pathogenic Variant c.5257C>T in the NBEAL2 Gene
• High molecular diagnostic yields and novel phenotypic expansions involving syndromic anorectal malformations
• Human Genetics of Hypoplastic Left Heart Syndrome
• Hybrid Renal Cortical Imaging with Single Photon Emission Computerized Tomography/Computed Tomography in a Pediatric Patient with Severe Caudal Regression Syndrome
• In vitro fertilization outcomes in VACTERL association (vertebral defects, anal atresia, cardiac defects, tracheoesophageal fistula, renal anomalies and limb anomalies): report of 2 cases
• Is horseshoe lung a component of VACTERL spectrum? Case report and review of literature
• Long-term urology outcomes of anorectal malformation
• Microdeletion on Xq27.1 in a Chinese VACTERL-Like Family with Kidney and Anal Anomalies
• NAD+ deficiency in human congenital malformations and miscarriage: A new model of pleiotropy
• Neurodevelopmental outcomes in individuals with VACTERL association. A population-based cohort study
• Nonfamilial VACTERL-H Syndrome in a Dizygotic Twin: Prenatal Ultrasound and Postnatal 3D CT Findings
• Omenn syndrome in a 10-month-old male with athymia and VACTERL association
• Outcome of Newborns with Tracheoesophageal Fistula: An Experience from a Rapidly Developing Country: Room for Improvement
• Patterns of multiple congenital anomalies in the National Birth Defect Prevention Study: Challenges and insights
• Pelvic Kidney
• Perioperative management of a parturient with VACTERL association for a caesarean section
• Persistent Urogenital Sinus Leading to Hydrometrocolpos in a Female Child With Features of McKusick-Kaufman Syndrome
• Post-herniorrhaphy extubation technique in pediatric patient with congenital diaphragmatic hernia and VACTERL association: A case report
• Predictors of poor outcomes in children with tracheoesophageal fistula/oesophageal atresia: an Australian experience
• Preliminary Experience With Quadratus Lumborum Catheters for Postoperative Pain Management in Pediatric-Aged Patients With Contraindications to Epidural Anesthesia
• Prenatal Diagnosis and Outcome of Scimitar Syndrome: A Case Series of Six Patients
• Prenatal diagnosis of distal 13q deletion syndrome in a fetus with esophageal atresia: a case report and review of the literature
• Prenatal diagnosis of VACTERL association after early-first trimester SARS-COV-2 infection
• Prenatal diagnosis of VACTERL association in the first trimester
• Presence of Cervical Vertebral Anomalies with Concomitant Non-Communicating Hydrocephalus and Multicystic Kidney in a Female Fetus: Where VACTERL-H Meets MURCS
• Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformation
• Renal Cell Carcinoma in a Patient With Crossed Renal Ectopia: A Case Report
• Respiratory failure in a patient with VACTERL association and concomitant spinal muscular atrophy
• Retrospective evaluation of clinical and molecular data of 148 cases of esophageal atresia
• Right Pulmonary Artery Originating from Ascending Aorta (Hemitruncus Arteriosus) with VACTERL Association in a Neonate: A Case Report
• SALL4 deletion and kidney and cardiac defects associated with VACTERL association
• Screening for VACTERL Anomalies in Children with Anorectal Malformations: Outcomes of a Standardized Approach
• Spectrum of fetal limb anomalies
• Substantial incidence of bladder dysfunction in patients with VACTERL association: Implications for surveillance
• Successful Repair of TEF and DORV in a Child in a Resource-Limited Setting
• Survival and factors associated with mortality among infants with anorectal malformation: a population-based study from a middle-income country
• Swallowing-related quality of life in children with oesophageal atresia: a national cohort study
• Syndromic and single gene disorders associated with fetal megacystis (I): Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS)
• Terminal myelocystocele: Surgical management
• The Importance of Screening for Additional Anomalies in Patients with Anorectal Malformations: A Retrospective Cohort Study
• The Incidence of Associated Anomalies in Children with Congenital Duodenal Obstruction-A Retrospective Cohort Study of 112 Patients
• Tracheal agenesis versus tracheal atresia: anatomical conditions, pathomechanisms and causes with a possible link to a novel MAPK11 variant in one case
• Understanding of the transition to adult healthcare services among individuals with VACTERL association in Sweden: A qualitative study
• Unicornuate uterus with a rudimentary non-communicating cavitary horn in association with VACTERL association: a rare case report
• VACTERL association in a fetus with multiple congenital malformations - Case report
• VACTERL Association in Patients With Metopic Synostosis: Is There a Link?
• VACTERL Association with Dorsal Pancreatic Agenesis
• Vacterl syndrome: Medical and stomatological considerations for comprehensive patient management
• Vertebral anomalies and VACTERL association in pontine tegmental cap dysplasia: a paediatric case report
• Wandering Spleen in a Patient With Significant Medical History