Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly-Reference-Cited by-同舟云学术

Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly

Published:2021-10-05 Issue:11 Volume:9 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Mohamed Amal M.¹^ORCID,Kamel Alaa K.¹,Eid Maha M.¹,Eid Ola M.¹,Mekkawy Mona¹,Hussein Shymaa H.¹,Zaki Maha S.²,Esmail Samira²,Afifi Hanan H.²^ORCID,El‐Kamah Ghada Y.²,Otaify Ghada A.²,El‐Awady Heba Ahmed³^ORCID,Elaidy Aya²,Essa Mahmoud Y.²,El‐Ruby Mona²,Ashaat Engy A.²,Hammad Saida A.¹,Mazen Inas²,Abdel‐Salam Ghada M. H.²,Aglan Mona²,Temtamy Samia²

Affiliation:

1. Division of Human Genetics and Genome Research Department of Human Cytogenetics National Research Centre Cairo Egypt

2. Division of Human Genetics and Genome Research Department of Clinical Genetics National Research Centre Cairo Egypt

3. Department of Pediatrics Faculty of Medicine Fayoum University Fayoum Egypt

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1829

Reference37 articles.

1. Case Report Familial balanced translocation leading to an offspring with phenotypic manifestations of 9p syndrome