Genome-Wide Detection of Uniparental Disomy in a Fetus with Intrauterine Growth Restriction Using Genotyping Microarrays

Author:

Soong Yung-Kuei,Wang Tzu-Hao,Lee Yun-Shien,Chen Chih-Ping,Chang Chia-Lin,Ho Szu-Ying,Chao An-Shine,Cheng Po-Jen,Chang Shuenn-Dyh

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference28 articles.

1. American College of Medical Genetics statement of diagnostic testing for uniparental disomy;Shaffer;Genet Med,2001

2. Uniparental disomy as a mechanism for human genetic disease;Spence;Am J Hum Genet,1988

3. Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization;Wolstenholme;Prenat Diagn,1996

4. Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction;Robinson;Am J Hum Genet,1997

5. Confined placental mosaicism and intrauterine fetal growth;Lestou;Arch Dis Child Fetal Neonatal Ed,1998

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