8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects-Reference-Cited by-同舟云学术

8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects

Published:2021-09-22 Issue:11 Volume:9 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Ben Ayed Ikhlas¹²^ORCID,Bouzid Amal¹³,Kammoun Fatma⁴⁵,souissi Amal¹,Jallouli Olfa⁴⁵,Mallouli Salma⁴⁵,Guidara Souhir²⁶,Loukil Salma¹,Aloulou Hajer⁷,Jbeli Fida¹,Aouichaoui Sahar²,Abid Dorra⁸,Abdelhedi Fatma²⁶,Triki Chahnez⁴⁵,Kamoun Hassen²⁶,Masmoudi Saber¹

Affiliation:

1. Laboratory of Molecular and Cellular Screening Processes (LPCMC) Center of Biotechnology of Sfax University of Sfax Sfax Tunisia

2. Medical Genetics Department University Hedi Chaker Hospital of Sfax Sfax Tunisia

3. Sharjah Institute for Medical Research College of Medicine University of Sharjah Sharjah United Arab Emirates

4. Child Neurology Department University Hedi Chaker Hospital of Sfax Sfax Tunisia

5. Research Laboratory Sfax University Sfax Tunisia

6. Laboratory of Human Molecular Genetics LR33ES99, Faculty of Medicine of Sfax University of Sfax Sfax Tunisia

7. Pediatric Department Hedi Chaker University HospitalUniversity of Sfax Sfax Tunisia

8. Cardiology Department Hedi Chaker University HospitalUniversity of Sfax Sfax Tunisia

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1811

Reference32 articles.

1. Mitochondrial Dysfunction in a Patient with 8q21.11 Deletion and Charcot-Marie-Tooth Disease Type 2K due to GDAP1 Haploinsufficiency

2. Familial occurrence of ptosis, nasal speech, prominent ears, hand anomalies and learning problems

3. Evening use of light-emitting eReaders negatively affects sleep, circadian timing, and next-morning alertness

4. RNA-Seq analysis of Gtf2ird1 knockout epidermal tissue provides potential insights into molecular mechanisms underpinning Williams-Beuren syndrome

5. DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

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