Natural histories of patients with Wolf‐Hirschhorn syndrome derived from variable chromosomal abnormalities-Reference-Cited by-同舟云学术

Natural histories of patients with Wolf‐Hirschhorn syndrome derived from variable chromosomal abnormalities

Published:2018-11-15 Issue:5 Volume:59 Page:169-173
ISSN:0914-3505
Container-title:Congenital Anomalies
language:en
Short-container-title:Congenit Anom

Author:

Yamamoto‐Shimojima Keiko¹,Kouwaki Masanori²,Kawashima Yuki³,Itomi Kazuya⁴,Momosaki Ken⁵,Ozasa Shiro⁵,Okamoto Nobuhiko⁶^ORCID,Yokochi Kenji⁷,Yamamoto Toshiyuki¹^ORCID

Affiliation:

1. Institute of Medical GeneticsTokyo Women's Medical University Tokyo Japan

2. Department of NeonatologyToyohashi Municipal Hospital Toyohashi Japan

3. Department of PediatricsTottori University Yonago Japan

4. Department of NeurologyAichi Children's Health and Medical Center Obu Japan

5. Department of PediatricsKumamoto University Kumamoto Japan

6. Department of Medical GeneticsOsaka Women's and Children's Hospital Osaka Japan

7. Department of PediatricsSeirei Mikatahara General Hospital Hamamatsu Japan

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cga.12318

Reference11 articles.

1. Wolf-Hirschhorn syndrome: A review and update

2. Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf–Hirschhorn Syndrome

3. Microarray and FISH-based genotype-phenotype analysis of 22 Japanese patients with Wolf-Hirschhorn syndrome

4. On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: Genotype-phenotype correlation analysis of 80 patients and literature review

5. Growth profiles of 34 patients with Wolf-Hirschhorn syndrome

Cited by 6 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. Wolf-Hirschhorn syndrome candidate 1 (Whsc1) methyltransferase signals via a Pitx2-miR-23/24 axis to effect tooth development;Journal of Biological Chemistry;2023-11

2. Identification of small-sized intrachromosomal segments at the ends of INV–DUP–DEL patterns;Journal of Human Genetics;2023-07-10

3. Prenatal phenotype of Wolf–Hirschhorn syndrome: A case series and literature review;Molecular Genetics & Genomic Medicine;2023-02-27

4. Bi-allelic LETM1 variants perturb mitochondrial ion homeostasis leading to a clinical spectrum with predominant nervous system involvement;The American Journal of Human Genetics;2022-09

5. Comprehending fibroblast growth factor receptor like 1: Oncogene or tumor suppressor?;Cancer Treatment and Research Communications;2021