MonoallelicBUB1B mutations and defective mitotic-spindle checkpoint in seven families with premature chromatid separation (PCS) syndrome-Reference-Cited by-同舟云学术

MonoallelicBUB1B mutations and defective mitotic-spindle checkpoint in seven families with premature chromatid separation (PCS) syndrome

Published:2006-02-15 Issue:4 Volume:140A Page:358-367
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Matsuura Shinya,Matsumoto Yoshiyuki,Morishima Ken-ichi,Izumi Hideki,Matsumoto Hiroshi,Ito Emi,Tsutsui Keisuke,Kobayashi Junya,Tauchi Hiroshi,Kajiwara Yoshinori,Hama Seiji,Kurisu Kaoru,Tahara Hidetoshi,Oshimura Mitsuo,Komatsu Kenshi,Ikeuchi Tatsuro,Kajii Tadashi

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference17 articles.

1. Immortalization of Human Uterine Leiomyoma and Myometrial Cell Lines After Induction of Telomerase Activity: Molecular and Phenotypic Characteristics

2. Prenatal diagnosis of premature centromere division–related mosaic variegated aneuploidy

3. Centromeres and Kinetochores

4. Temporal and spatial control of cyclin B1 destruction in metaphase

5. Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B

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