Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2001.590410.x/fullpdf
Reference26 articles.
1. A further whole arm 1;19 translocation with alpha-satellite DNA breakage;Diaz-Castanos;Genet Couns,1997
2. Balanced nonacrocentric whole-arm reciprocal translocations: a de novo case and literature review;Farrell;Am J Med Genet,1995
3. Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with α-satellite DNA probes;Tharapel;Am J Med Genet,1991
4. Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p;Wang;Am J Med Genet,1997
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1. 18p Deletion Syndrome Originating from Rare Unbalanced Whole-Arm Translocation between Chromosomes 13 and 18: A Case Report and Literature Review;Children;2022-07-01
2. Human Chromosome 18 and Acrocentrics: A Dangerous Liaison;International Journal of Molecular Sciences;2021-05-26
3. The genotype and phenotype of chromosome 18p deletion syndrome;Medicine;2021-05-07
4. Prenatal diagnosis of de novo monosomy 18p deletion syndrome by chromosome microarray analysis;Medicine;2019-04
5. Prenatal diagnosis of holoprosencephaly with proboscis and cyclopia caused by monosomy 18p resulting from unbalanced whole-arm translocation of 18;21;Case Reports in Perinatal Medicine;2016-03-01
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