Your browser doesn't support javascript.
loading
Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly.
Mohamed, Amal M; Kamel, Alaa K; Eid, Maha M; Eid, Ola M; Mekkawy, Mona; Hussein, Shymaa H; Zaki, Maha S; Esmail, Samira; Afifi, Hanan H; El-Kamah, Ghada Y; Otaify, Ghada A; El-Awady, Heba Ahmed; Elaidy, Aya; Essa, Mahmoud Y; El-Ruby, Mona; Ashaat, Engy A; Hammad, Saida A; Mazen, Inas; Abdel-Salam, Ghada M H; Aglan, Mona; Temtamy, Samia.
Affiliation
  • Mohamed AM; Division of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, Cairo, Egypt.
  • Kamel AK; Division of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, Cairo, Egypt.
  • Eid MM; Division of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, Cairo, Egypt.
  • Eid OM; Division of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, Cairo, Egypt.
  • Mekkawy M; Division of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, Cairo, Egypt.
  • Hussein SH; Division of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, Cairo, Egypt.
  • Zaki MS; Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • Esmail S; Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • Afifi HH; Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • El-Kamah GY; Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • Otaify GA; Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • El-Awady HA; Department of Pediatrics, Faculty of Medicine, Fayoum University, Fayoum, Egypt.
  • Elaidy A; Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • Essa MY; Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • El-Ruby M; Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • Ashaat EA; Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • Hammad SA; Division of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, Cairo, Egypt.
  • Mazen I; Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • Abdel-Salam GMH; Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • Aglan M; Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • Temtamy S; Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
Mol Genet Genomic Med ; 9(11): e1829, 2021 11.
Article in En | MEDLINE | ID: mdl-34609792
Subject(s)
Key words
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Database: MEDLINE Main subject: Chromosome Deletion / Craniosynostoses Type of study: Prognostic_studies Limits: Humans Country/Region as subject: Africa Language: En Year: 2021 Type: Article
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Database: MEDLINE Main subject: Chromosome Deletion / Craniosynostoses Type of study: Prognostic_studies Limits: Humans Country/Region as subject: Africa Language: En Year: 2021 Type: Article