Long‐term remission of bilateral Wilms tumors that developed from premature separation of chromatids/mosaic variegated aneuploidy syndrome due to bilateral nephrectomy and peritoneal dialysis-Reference-Cited by-同舟云学术

Long‐term remission of bilateral Wilms tumors that developed from premature separation of chromatids/mosaic variegated aneuploidy syndrome due to bilateral nephrectomy and peritoneal dialysis

Published:2019-05-13 Issue:8 Volume:66 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Ochiai Kayo¹,Yamada Ai¹,Kimoto Yasuhiro¹,Imamura Hideaki¹,Ikeda Toshio¹^ORCID,Matsukubo Makoto²,Ieiri Satoshi²,Moritake Hiroshi¹^ORCID

Affiliation:

1. Division of Pediatrics, Faculty of MedicineUniversity of Miyazaki Miyazaki, Japan

2. Department of Pediatric SurgeryKagoshima University Kagoshima, Japan

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.27804

Reference15 articles.

1. Mosaic variegated aneuploidy with multiple congenital abnormalities: Homozygosity for total premature chromatid separation trait

2. Chromosomal Instability Syndrome of Total Premature Chromatid Separation with Mosaic Variegated Aneuploidy Is Defective in Mitotic-Spindle Checkpoint

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

4. TALEN-mediated single-base-pair editing identification of an intergenic mutation upstream of BUB1B as causative of PCS (MVA) syndrome

5. Cancer-prone syndrome of mosaic variegated aneuploidy and total premature chromatid separation: Report of five infants

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