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Cited by 224

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Preimplantation genetic diagnosis for aneuploidy screening in early human embryos: a review

Wilton, Leeanda·2002·Prenatal Diagnosis

Abstract

Embryonic aneuploidies may be responsible for pregnancy failure in many IVF patients. In recent years, fluorescent in situ hybridisation (FISH) for multiple chromosomes has been used to document a high frequency of chromosomal errors and aneuploidy in human preimplantation embryos and, after embryo biopsy, to select embryos that are more likely to implant. Such studies suggest that women with recurrent miscarriage and advanced maternal age may benefit most from preimplantation genetic diagnosis with aneuploidy screening (PGD‐AS). The success of PGD‐AS is likely to be enhanced by new technologies, such as comparative genomic hybridisation, which enable full karyotyping of single cells. Copyright © 2002 John Wiley & Sons, Ltd.

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Metadata

Authors
Wilton, L.
Venue
Prenatal Diagnosis
Publisher
Wiley
Published
2002-06
Volume
22
Issue
6
Pages
512-518
ISSN
  • 0197-3851 (ISSN-L)
  • 1097-0223
OpenAlex
W2028645337
Cited by
224
References
1
FWCI
10.26
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Preimplantation genetic diagnosis for aneuploidy screening in early human embryos: a review. https://app.cochat.ai/papers/10.1002/pd.388
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Wilton, L. (2002). Preimplantation genetic diagnosis for aneuploidy screening in early human embryos: a review. Prenatal Diagnosis. https://doi.org/10.1002/pd.388

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