Using Array-Based Comparative Genomic Hybridization to Diagnose Pallister-Killian Syndrome-Reference-Cited by-同舟云学术

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Using Array-Based Comparative Genomic Hybridization to Diagnose Pallister-Killian Syndrome

Published:2017-01-01 Issue:1 Volume:37 Page:66-70
ISSN:2234-3806
Container-title:Annals of Laboratory Medicine
language:en
Short-container-title:Ann Lab Med

Author:

Lee Mi-Na¹,Lee Jiwon²,Yu Hee Joon²,Lee Jeehun²,Kim Sun-Hee³

Affiliation:

1. Green Cross Laboratories, Yongin, Korea

2. Departments of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

3. Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

Publisher

Annals of Laboratory Medicine

Subject

Biochemistry, medical,Clinical Biochemistry,General Medicine

Link

http://synapse.koreamed.org/pdf/10.3343/alm.2017.37.1.66

Reference20 articles.

1. Pallister-Killian syndrome: cytogenetic and molecular studies

2. Mosaicism in Pallister i(12p) syndrome

3. Tetrasomy 12p (Pallister-Killian syndrome).

4. Novel clinical manifestations in Pallister-Killian syndrome: Comprehensive evaluation of 59 affected individuals and review of previously reported cases

Cited by 7 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. Pallister-Killian syndrome;Cases in Laboratory Genetics and Genomics (LGG) Practice;2023

2. Polymicrogyria with calcification in Pallister-Killian syndrome detected by microarray analysis;Brain and Development;2021-03

3. PALLISTER–KILLIAN SYNDROME;Cassidy and Allanson's Management of Genetic Syndromes;2020-10-30

4. Hypotonic infant with Pallister–Killian syndrome diagnosed by cytogenetic microarray, without pigmentary skin changes and malformations;Journal of Genetics;2020-04-20

5. Postnatal clinical phenotype of five patients with Pallister–Killian Syndrome (tetrasomy 12p): Interest of array CGH for diagnosis and review of the literature;Molecular Genetics & Genomic Medicine;2019-08-27

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