Beckwith-Wiedemann Syndrome and Jacobsen Syndrome Caused by 11pter Duplication and 11qter Deletion Inherited from Paternal Pericentric Inversion-Reference-Cited by-同舟云学术

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Beckwith-Wiedemann Syndrome and Jacobsen Syndrome Caused by 11pter Duplication and 11qter Deletion Inherited from Paternal Pericentric Inversion

Published:2020-07-01 Issue:3 Volume:10 Page:255-261
ISSN:2093-6338
Container-title:Laboratory Medicine Online
language:en
Short-container-title:Lab Med Online

Author:

Choi Won-Kyu¹,Lim Sung-Eun²,Kim Gu-Hwan²,Lee Beom-Hee²³,Seol Chang-An¹²,Seo Eul-Ju¹²^ORCID

Affiliation:

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

2. Medical Genetics Center, Asan Medical Center, Seoul, Korea

3. Department of Pediatrics, University of Ulsan College of Medicine and Asan Medical Center Children’s Hospital, Seoul, Korea

Publisher

Laboratory Medicine Online

Subject

Industrial and Manufacturing Engineering

Link

https://pdf.medrang.co.kr/LMO/2020/010/LMO010-03-12.pdf

Reference13 articles.

1. Chromosome Abnormalities and Genetic Counseling

2. Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement

3. Beckwith-Wiedemann syndrome

4. Beckwith–Wiedemann syndrome

5. The 11q terminal deletion disorder: A prospective study of 110 cases

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