Diagnostic Usefulness of MLPA Techniques for Recurrent Copy Number Variants Detection in Global Developmental Delay/Intellectual Disability-Reference-Cited by-同舟云学术

Diagnostic Usefulness of MLPA Techniques for Recurrent Copy Number Variants Detection in Global Developmental Delay/Intellectual Disability

Published:2021-08 Issue: Volume:Volume 14 Page:4511-4515
ISSN:1178-7074
Container-title:International Journal of General Medicine
language:en
Short-container-title:IJGM

Author:

Miclea Diana,Szucs Adriana,Mirea Andreea^ORCID,Stefan Delia-Maria,Nazarie Florina,Bucerzan Simona,Lazea Cecilia^ORCID,Grama Alina,Pop Tudor Lucian^ORCID,Farcas Marius^ORCID,Zaharie Gabriela^ORCID,Matyas Melinda,Mager Monica,Vintan Mihaela^ORCID,Popp Radu,Alkhzouz Camelia

Publisher

Informa UK Limited

Subject

General Medicine

Reference22 articles.

1. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. American Psychiatric Association;2013:271–279. Available from: https://psychiatryonline.org/doi/book/10.1176/appi.books.9780890425596. Accessed March 1, 2020.

2. Practice parameter: Evaluation of the child with global developmental delay [RETIRED]

3. Comprehensive Evaluation of the Child With Intellectual Disability or Global Developmental Delays

4. New generation sequencing for the diagnosis of intellectual disabilities: Exome sequencing or large panel?

5. Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

Cited by 4 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. MECP2-gén-duplikáció gyermekkori és praenatalis diagnózisa;Orvosi Hetilap;2024-01-07

2. Multiple congenital anomalies and developmental delay;Cases in Laboratory Genetics and Genomics (LGG) Practice;2023

3. Copy number variation analysis in 189 Romanian patients with global developmental delay/intellectual disability;Italian Journal of Pediatrics;2022-12-30

4. Pathogenic Copy Number Variations Involved in the Genetic Etiology of Syndromic and Non-Syndromic Intellectual Disability—Data from a Romanian Cohort;Diagnostics;2022-12-12