Clinical findings and molecular cytogenetic study of de novo pure chromosome 9p deletion: Pre- and postnatal diagnosis
Objective: The aim of this report is to describe the phenotype-genotype correlation of chromosome 9p deletion syndrome cases, particularly the prenatal cases. Case report: We present a female fetus at 17+4 weeks of gestation age detected with an 8 × 6 mm2 omphalocele. Karyotype analysis of the fetus...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Elsevier,
2016-12-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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