Sacral Dysgenesis Associated with Terminal Deletion of Chromosome 7 (q36-qter)
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference13 articles.
1. Different proximal and distal rearrangements of chromosome 7q associated with holoprosencephaly;Benzacken;J Med Genet,1997
2. Strong variable clinical presentation in 3 patients with 7q terminal deletion;Frints;Genet Couns,1998
3. Two unrelated cases of single maxillary central incisor with 7q terminal deletion;Masuno;Jpn J Hum Genet,1990
4. Terminal deletion of the chromosome 7(q36–qter) in an infant with sacral agenesis and anterior myelomeningocele;Rodriguez;Am J Med Genet,2002
5. Minimal clinical expression of the holoprosencephaly spectrum and of currarino syndrome due to different cytogenetic rearrangements deleting the sonic hedgehog gene and the HLXB9 gene at 7q36.3;Horn;Am J Med Genet A,2004
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1. Prenatal detection of chromosome 7q deletion with duplication and literature review;2024-01-03
2. Prenatal ultrasound-assisted identification of multiple malformations caused by a deletion in the long-arm end of chromosome 7 and review of the literature;The Journal of Maternal-Fetal & Neonatal Medicine;2020-11-19
3. Elongated Conus Medullaris, Sacral Agenesis, and Scoliosis: A Case Report of a Patient with Trisomy 19q and Monosomy 7q;World Neurosurgery;2019-04
4. Urine retention as the first presentation of congenital absence of the sacrum;Medicine;2018-08
5. Kaposi sarcoma, oral malformations, mitral dysplasia, and scoliosis associated with 7q34-q36.3 heterozygous terminal deletion;American Journal of Medical Genetics Part A;2017-05-09
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