A Clinical and Molecular Description of a Rare Case of Chromosomal Abnormality (Partial Trisomy 14q11.2-q21.1 and Partial Monosomy 21q11.2-q21.3)
The article presents a detailed clinical and molecular and cytogenetic analysis of the unique case of a rare chromosomal abnormality (duplication of 14q11.2-q21.1 and deletion of 21q11.2-q21.3). This chromosomal abnormality is a result of segregation (2:2) of a balanced chromosomal translocation in...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
"Paediatrician" Publishers LLC,
2016-08-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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