7q Deletion/12q Duplication Is the Possible Cause of an Alobar Holoprosencephaly Case-Reference-Cited by-同舟云学术

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7q Deletion/12q Duplication Is the Possible Cause of an Alobar Holoprosencephaly Case

Published:2017-11-24 Issue:1 Volume:9 Page:52-57
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Paspaliaris Vassilis,Vrachnis Nikolaos,Iliodromiti Zoe,Antonakopoulos Nikolaos,Papaioannou Giorgos,Vlachadis Nikolaos,Anastasiadou Foteini,Sotiriou Sotirios,Garas Antonios,Thomaidis Lorreta,Manolakos Emmanouil

Publisher

S. Karger AG

Subject

Genetics(clinical),Genetics

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. De novo 7q11.21 duplication with 4-hydroxy phenylacetic aciduria– A rare neurodevelopmental syndrome: A Case report;2023-10-04

2. Duplication of 12q24.21q24.33 in a Girl with Epilepsy, Expanding the Phenotype;Molecular Syndromology;2022

3. 7q31.32 partial duplication: First report of a child with dysmorphism, autistic spectrum disorder, moderate intellectual disability and, epilepsy. Literature review;Epilepsy Research;2019-12

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