Exome Sequencing Identifies Multiple Genetic Diagnoses in Children with Syndromic Growth Disorders-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Exome Sequencing Identifies Multiple Genetic Diagnoses in Children with Syndromic Growth Disorders

Published:2024-02 Issue: Volume:265 Page:113841
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Rezende Raissa Carneiro^ORCID,Menezes de Andrade Nathalia Liberatoscioli^ORCID,Branco Dantas Naiara Castelo^ORCID,de Polli Cellin Laurana^ORCID,Victorino Krepischi Ana Cristina^ORCID,Lerario Antonio Marcondes^ORCID,de Lima Jorge Alexander Augusto^ORCID

Funder

FAPESP

CAPES

CNPq

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference36 articles.

1. Genetic disorders in prenatal onset syndromic short stature identified by exome sequencing;Homma;J Pediatr,2019

2. Genetic investigation of patients with tall stature;de Albuquerque Albuquerque;Eur J Endocrinol,2020

3. Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature;Hauer;Genet Med,2018

4. High frequency of genetic/epigenetic disorders in short-stature children born with very low birth weight;Freire;Am J Med Genet A,2022

5. Genetic short stature;Grunauer;Growth Horm IGF Res,2018

Cited by 2 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. Genetic Findings in Short Turkish Children Born to Consanguineous Parents;Hormone Research in Paediatrics;2024-06-05

2. La pagina gialla;Medico e Bambino;2024-02-23

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP