Partial Trisomy 1q41 Syndrome Delineated by Whole Genomic Array Comparative Genome Hybridization-Reference-Cited by-同舟云学术

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Partial Trisomy 1q41 Syndrome Delineated by Whole Genomic Array Comparative Genome Hybridization

Published:2008 Issue:6 Volume:23 Page:1097
ISSN:1011-8934
Container-title:Journal of Korean Medical Science
language:en
Short-container-title:J Korean Med Sci

Author:

Shin Yong Beom¹,Nam Sang Ook²,Seo Eul-Ju³,Kim Hyung-Hoi⁴,Chang Chulhun L.⁴,Lee Eun-Yup⁴,Son Han-Chul⁴,Hwang Sang-Hyun⁴⁵

Affiliation:

1. Department of Rehabilitation Medicine, Pusan National University, School of Medicine, Busan, Korea.

2. Department of Pediatrics, Pusan National University, School of Medicine, Busan, Korea.

3. Department of Laboratory Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

4. Department of Laboratory Medicine, Pusan National University, School of Medicine, Busan, Korea.

5. Medical Research Institute, Pusan National University, Busan, Korea.

Publisher

Korean Academy of Medical Sciences

Subject

General Medicine

Link

https://synapse.koreamed.org/pdf/10.3346/jkms.2008.23.6.1097

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identification of Balanced and Unbalanced Complex Chromosomal Rearrangement Involving Chromosomes 1, 11, and 15;Cureus;2021-07-04

2. Myelodysplastic syndrome in an infant with constitutional pure duplication 1q41-qter;Human Genome Variation;2018-05-21

3. Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes;BMC Medical Genomics;2014-09-15

4. Miller-Dieker Syndrome with der(17)t(12;17)(q24.33;p13.3)pat Presenting with a Potential Risk of Mis-identification as a de novo Submicroscopic Deletion of 17p13.3;Annals of Laboratory Medicine;2011-01-01

5. A Case of Partial Trisomy 2p23-pter Syndrome with Trisomy 18p Due to a de novo Supernumerary Marker Chromosome;Annals of Laboratory Medicine;2010-06-01

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