Noninvasive prenatal testing aids identification of tetrasomy 18p: A case report
Tetrasomy 18p syndrome (Online Mendelian Inheritance in Man 614290) is a rare chromosomal disorder that is seen in approximately 1 in every 180,000 live births. It is caused by the presence of isochromosome 18p, which is a supernumerary marker composed of two copies of the short arms of chromosome 1...
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| Main Authors: | , , , , |
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| Format: | Book |
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Elsevier,
2020-07-01T00:00:00Z.
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