Cytogenetic and molecular analysis in trisomy 12p
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference32 articles.
1. Isolation and subregional mapping of a human cDNA clone detecting a common RELP on chromosome 12
2. Polymorphic DNA region adjacent to the 5' end of the human insulin gene.
3. Partial trisomy 12p due to t(12;21)pat translocation
4. Peripherin gene is linked to keratin 18 gene on human chromosome 12
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1. Non-mosaic partial duplication 12p in a patient with dysmorphic characteristics and developmental delay;Genetics and Molecular Biology;2020
2. Molecular Delineation of Partial Trisomy 14q and Partial Trisomy 12p in a Patient with Dysmorphic Features, Heart Defect and Developmental Delay;Cytogenetic and Genome Research;2015
3. Nonmosaic partial duplication 12p;Medical Research Journal;2014-12
4. Variable levels of tissue mosaicism can confound the interpretation of chromosomal microarray results from peripheral blood;European Journal of Medical Genetics;2014-05
5. Report on 3 patients with 12p duplication including GRIN2B;European Journal of Medical Genetics;2014-04
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