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Prenatal Diagnosis Using Chromosomal Microarray Analysis in High-Risk Pregnancies.

J Clin Med · 2022 · PMC9267905 · PMID 35806909

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Clinics and laboratories should report female carriers of X-linked recessive mutations associated with childhood-onset disorders, since there may be significant risk to the family if affected males are conceived [ 21 ].

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.