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Clinical and genetic characterization of ten Egyptian patients with Wolf-Hirschhorn syndrome and review of literature.
Mekkawy, Mona K; Kamel, Alaa K; Thomas, Manal M; Ashaat, Engy A; Zaki, Maha S; Eid, Ola M; Ismail, Samira; Hammad, Saida A; Megahed, Hisham; ElAwady, Heba; Refaat, Khaled M; Hussien, Shymaa; Helmy, Nivine; Abd Allah, Sally G; Mohamed, Amal M; El Ruby, Mona O.
Affiliation
  • Mekkawy MK; Human Cytogenetics Department, National Research Centre, Cairo, Egypt.
  • Kamel AK; Human Cytogenetics Department, National Research Centre, Cairo, Egypt.
  • Thomas MM; Clinical Genetics Department, National Research Centre, Cairo, Egypt.
  • Ashaat EA; Clinical Genetics Department, National Research Centre, Cairo, Egypt.
  • Zaki MS; Clinical Genetics Department, National Research Centre, Cairo, Egypt.
  • Eid OM; Human Cytogenetics Department, National Research Centre, Cairo, Egypt.
  • Ismail S; Clinical Genetics Department, National Research Centre, Cairo, Egypt.
  • Hammad SA; Clinical Genetics Department, National Research Centre, Cairo, Egypt.
  • Megahed H; Clinical Genetics Department, National Research Centre, Cairo, Egypt.
  • ElAwady H; Pediatric Department, Faculty of Medicine, Fayoum unIversity, Fayoum, Egypt.
  • Refaat KM; Human Cytogenetics Department, National Research Centre, Cairo, Egypt.
  • Hussien S; Human Cytogenetics Department, National Research Centre, Cairo, Egypt.
  • Helmy N; Human Cytogenetics Department, National Research Centre, Cairo, Egypt.
  • Abd Allah SG; Human Cytogenetics Department, National Research Centre, Cairo, Egypt.
  • Mohamed AM; Human Cytogenetics Department, National Research Centre, Cairo, Egypt.
  • El Ruby MO; Clinical Genetics Department, National Research Centre, Cairo, Egypt.
Mol Genet Genomic Med ; 9(2): e1546, 2021 02.
Article in En | MEDLINE | ID: mdl-33217222
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Wolf-Hirschhorn Syndrome / Genotype Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Mol Genet Genomic Med Year: 2021 Type: Article Affiliation country: Egypt
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Wolf-Hirschhorn Syndrome / Genotype Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Mol Genet Genomic Med Year: 2021 Type: Article Affiliation country: Egypt