Disease: VACTERL association with hydrocephaly- X-linked
- A novel murine allele of Intraflagellar Transport Protein 172 causes a syndrome including VACTERL-like features with hydrocephalus
- Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome
- Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort
- Mermaid syndrome associated with VACTERL-H syndrome
- Nonfamilial VACTERL-H Syndrome in a Dizygotic Twin: Prenatal Ultrasound and Postnatal 3D CT Findings
- Presence of Cervical Vertebral Anomalies with Concomitant Non-Communicating Hydrocephalus and Multicystic Kidney in a Female Fetus: Where VACTERL-H Meets MURCS
- Sirenomelia: A Multi-systemic Polytopic Field Defect with Ongoing Controversies
- Syringomyelia in VACTERL-H association: a new neurological feature in an adult patient
- Thinking of VACTERL-H? Rule out Fanconi Anemia according to PHENOS
- Unusual branchial arch, dermoepidermal and nervous system anomalies in a neonate with VACTERL-H syndrome
- VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer
- VACTERL with hydrocephalus and branchial arch defects: prenatal, clinical, and autopsy findings in two brothers
- VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance
- VACTERL-H association with tibial agenesis. Expansion of the clinical phenotype?
- VACTERL-H with triphalangeal thumb and hypothyroidism in a female patient
- VATER and hydrocephalus: distinct syndrome?
- X-linked recessive VACTERL-H due to a mutation in FANCB in a preterm boy
- X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations
- X-linked VACTERL-H caused by deletion of exon 3 in FANCB: A case report