Risk of Recurrence of Fetal Chromosomal Aberrations: Analysis of Trisomy 21, Trisomy 18, Trisomy 13, and 45,X in 1,076 Japanese Mothers

Author:

Uehara Shigeki,Yaegashi Nobuo,Maeda Tohru,Hoshi Nobuhiko,Fujimoto Seiichiro,Fujimori Keiya,Yanagida Kaoru,Yamanaka Michiko,Hirahara Fumiki,Yajima Akira

Publisher

Wiley

Subject

Obstetrics and Gynaecology

Reference23 articles.

1. Maternal age-specific rates of 47, + 21 and other cytogenetic abnormalities diagnosed in the first trimester of pregnancy in chorionic villus biopsy specimens: Comparison with rates expected from observations at amniocentesis;Hook;Am J Hum Genet,1988

2. Age-specific incidences of chromosome abnormalities at the second trimester amniocentesis for Japanese mothers aged 35 and older: Collaborative study of 5484 cases;Yaegashi;J Hum Genet,1998

3. Risk for chromosome abnormality at amniocentesis following a child with a non-inherited chromosome aberration. A European collaborative study on prenatal diagnoses 1981;Stene;Prenat Diag,1981

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2. Prenatal diagnosis and molecular genetic analysis of recurrent trisomy 18 of maternal origin in two consecutive pregnancies;Taiwanese Journal of Obstetrics and Gynecology;2023-05

3. Prenatal Diagnosis of Chromosomal Abnormalities through Chorionic Villus Sampling and Amniocentesis;Genetic Disorders and the Fetus;2021-04-20

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