A familial case of overgrowth syndrome caused by a 9q22.3 microdeletion in a mother and daughter-Reference-Cited by-同舟云学术

A familial case of overgrowth syndrome caused by a 9q22.3 microdeletion in a mother and daughter

Published:2020-05 Issue:5 Volume:63 Page:103872
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Yamada Hikari,Shimura Masaru,Takahashi Hidekuni,Nara Shonosuke,Morishima Yasuyuki,Go Soken,Miyashita Toshiyuki,Numabe Hironao,Kawashima Hisashi

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference17 articles.

1. The LIN28/let-7 pathway in cancer;Balzeau;Front. Genet.,2017

2. Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome;Boonen;Am. J. Med. Genet.,2005

3. Wilms tumor associated with the 9q22.3 microdeletion syndrome: 2 new case reports and a review of the literature;Cayrol;J. Pediatr. Hematol. Oncol.,2018

4. Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci;Garavelli;Am. J. Med. Genet.,2013

5. Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas;Isidor;Eur. J. Hum. Genet.,2013

Cited by 3 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. An investigation of the etiology and follow‐up findings in 35 children with overgrowth syndromes, including biallelic SUZ12 variant;American Journal of Medical Genetics Part A;2023-03-15

2. Genomics of human congenital hydrocephalus;Child's Nervous System;2021-07-07

3. Microdeletion of 9q22.3: A patient with minimal deletion size associated with a severe phenotype;American Journal of Medical Genetics Part A;2021-05-07