Myelodysplastic syndrome in an infant with constitutional pure duplication 1q41-qter-Reference-Cited by-同舟云学术

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Myelodysplastic syndrome in an infant with constitutional pure duplication 1q41-qter

Published:2018-05-21 Issue:1 Volume:5 Page:
ISSN:2054-345X
Container-title:Human Genome Variation
language:en
Short-container-title:Hum Genome Var

Author:

Morokawa Hirokazu,Kamiya Motoko,Wakui Keiko,Kobayashi Mikiko,Kurata Takashi,Matsuda Kazuyuki,Kawamura Rie,Kanno Hiroyuki,Fukushima Yoshimitsu,Nakazawa Yozo,Kosho Tomoki

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Biochemistry

Link

http://www.nature.com/articles/s41439-018-0008-8.pdf

Reference16 articles.

1. Kulikowski, L. D. et al. Pure duplication 1q41-qter: further delineation on trisomy 1q syndromes. Am. J. Med. Genet. A 146A, 2663–2667 (2008).

2. Shin, Y. B. et al. Partial trisomy 1q41 syndrome delineated by whole genomic array comparative genome hybridization. J. Korean Med. Sci. 23, 1097–1101 (2008).

3. Watanabe, S. et al. Detailed analysis of 26 cases of 1q partial duplication/triplication syndrome. Am. J. Med. Genet. A 170A, 908–917 (2016).

4. Vardiman, J. W. et al. The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes. Blood 114, 937–951 (2009).

5. Arber, D. A. et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood 127, 2391–2405 (2016).

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