The Use of Fluorescence In situ Hybridisation in the Diagnosis of Hidden Mosaicism in Egyptian Patients with Turner Syndrome

Background: Turner syndrome (TS) is the most common chromosomal abnormality in females. The diagnosis of TS is based on karyotyping of 30 blood lymphocytes. This technique does not rule out tissue mosaicism or low-grade mosaicism in the blood. Because of the associated risk of gonadoblastoma, mosaic...

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Hlavní autoři:	Heba Mohamed Ossama, Soha Kholeif, Ghada Mohamed Elhady
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Wolters Kluwer Medknow Publications 2023-10-01
Edice:	Journal of Human Reproductive Sciences
Témata:	fluorescent in situ hybridisation mosaicism turner syndrome
On-line přístup:	https://journals.lww.com/10.4103/jhrs.jhrs_128_23
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