Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference24 articles.
1. Partial trisomy of the long arm of chromosome 1 due to a familial translocation t (1; 10) (q32; q26);Bonfante;Hum Genet,1978
2. Trisomy (1q) (q42-qter): confirmation of a syndrome;Chia;Clin Genet,1988
3. Congenital ocular defects associated with an abnormality of the human chromosome 1: trisomy 1q32-qter;Clark;J Pediatr Ophthalmol Strabismus,1994
4. Detection of a de novo duplication of 1q32-qter by florescence in situ hybridization in a boy with multiple malformations: further delineation of the trisomy 1q syndrome;Duba;J Med Genet,1997
5. Prenatal diagnosis of partial trisomy 1q using florescence in situ hybridization;DuPont;Am J Med Genet,1994
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1. Developmental Delay and Rehabilitation in an Infant with Partial Trisomy 1q32.1 to 1q44: A Case Report;Neonatal Medicine;2022-05-31
2. Identification of Balanced and Unbalanced Complex Chromosomal Rearrangement Involving Chromosomes 1, 11, and 15;Cureus;2021-07-04
3. Proteinuric glomerulopathy in an adolescent with a distal partial trisomy chromosome 1;CEN Case Reports;2018-05-16
4. Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: Molecular cytogenetic analysis, fetal pathology and review of the literature;Birth Defects Research Part A: Clinical and Molecular Teratology;2014-02-12
5. Partial trisomy of the long arm of chromosome 1: Prenatal diagnosis, clinical evaluation and cytogenetic findings. Case report and review of the literature;Journal of Obstetrics and Gynaecology Research;2012-08-26
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