17q21.31 Microdeletion: Brain Anomalies Leading to Prenatal Diagnosis-Reference-Cited by-同舟云学术

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17q21.31 Microdeletion: Brain Anomalies Leading to Prenatal Diagnosis

Published:2014 Issue:3 Volume:144 Page:178-182
ISSN:1424-8581
Container-title:Cytogenetic and Genome Research
language:en
Short-container-title:Cytogenet Genome Res

Author:

Egloff Matthieu,Encha-Razavi Ferechte,Garel Catherine,Bonnière-Darcy Maryse,Millischer Anne-Elodie,Lapierre Jean-Michel,Fontaine Sophie,de Blois Marie-Christine,Vekemans Michel,Turleau Catherine,Ville Yves,Malan Valérie

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics,Molecular Biology

Cited by 11 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. The clinical phenotype of Koolen‐de Vries syndrome in Turkish patients and literature review;American Journal of Medical Genetics Part A;2023-04-13

2. The diagnosis of the first‐documented intragenic KANSL1 microduplication patient broadens the genetic spectrum of Koolen de Vries syndrome;Clinical Genetics;2022-02-22

3. Prenatal ultrasound findings in Koolen‐de Vries foetuses: Central nervous system anomalies are frequent markers of this syndrome;Molecular Genetics & Genomic Medicine;2021-03-18

4. Koolen‐de Vries syndrome: First report of two unrelated Indian patients;American Journal of Medical Genetics Part A;2020-12-08

5. Impact of polymorphic transposable elements on transcription in lymphoblastoid cell lines from public data;BMC Bioinformatics;2019-11

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