Open AccessFurther Phenotypic Delineation of Partial Trisomy 17q and Partial Monosomy 20q due to Rare t(17;20)
Author(s) -
Gizem Ürel Demir,
Özlem Akgün Doğan,
Sümeyra Oğuz,
Naz Güleray-Lafcı,
Pelin Özlem ŞimşekKiper,
Gülen Eda Ütine,
Mehmet Alikaşifoğlu,
Koray Boduroğlu
Publication year - 2020
Publication title -
molecular syndromology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.609
H-Index - 36
eISSN - 1661-8777
pISSN - 1661-8769
DOI - 10.1159/000505141
Subject(s) - intellectual disability , copy number variation , subtelomere , gene duplication , partial trisomy , microarray , monosomy , chromosomal translocation , genetics , comparative genomic hybridization , microarray analysis techniques , phenotype , trisomy , biology , etiology , medicine , chromosome , karyotype , gene , pathology , genome , gene expression
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