A 14q31.1-q32.11 deletion case: Genotype – Neurological Phenotype Correlations in 14q interstitial deletion syndrome-Reference-Cited by-同舟云学术

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A 14q31.1-q32.11 deletion case: Genotype – Neurological Phenotype Correlations in 14q interstitial deletion syndrome

Published:2020-06-06 Issue:3 Volume:25 Page:1677-1682
ISSN:1224-5984
Container-title:Romanian Biotechnological Letters
language:
Short-container-title:Rom Biotechnol Lett.

Author:

ROZA EUGENIA, ,STREAȚĂ IOANA,ȘOȘOI SIMONA,BURADA FLORIN,PUIU MARIA,IOANA MIHAI,TELEANU RALUCA IOANA

Publisher

Digital ProScholar Media

Subject

Agronomy and Crop Science,Genetics,Applied Microbiology and Biotechnology,Biotechnology

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. Copy number variations in autistic children;Biomedical Reports;2024-06-03

2. 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

3. Phenotypic and Genotypic Spectrum of Early-Onset Developmental and Epileptic Encephalopathies—Data from a Romanian Cohort;Genes;2022-07-15

4. The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients;Genes;2021-07-01

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