VACTERL with hydrocephalus and branchial arch defects: Prenatal, clinical, and autopsy findings in two brothers
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference13 articles.
1. VACTERL and hydrocephalus
2. VACTERL with hydrocephalus: A further case with probable autosomal recessive inheritance
3. Absence of excess chromosome breakage in a patient with VACTERL-hydrocephalus
4. VACTERL with hydrocephalus: Further delineation of the syndrome(s)
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1. Nonfamilial VACTERL-H Syndrome in a Dizygotic Twin: Prenatal Ultrasound and Postnatal 3D CT Findings;Medicina;2023-07-28
2. Hydrocephalus and genetic disorders;Cerebrospinal Fluid and Subarachnoid Space;2023
3. Presence of Cervical Vertebral Anomalies with Concomitant Non-Communicating Hydrocephalus and Multicystic Kidney in a Female Fetus: Where VACTERL-H Meets MURCS;Fetal and Pediatric Pathology;2021-10-23
4. A case of bilateral coronoid process hyperplasia in a child with suspected VACTERL-H syndrome;Japanese Journal of Oral and Maxillofacial Surgery;2018-10-20
5. Maternal drug use and the risk of anorectal malformations: systematic review and meta-analysis;Orphanet Journal of Rare Diseases;2018-05-10
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