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Cytogenomic characterization of 1q43q44 deletion associated with 4q32.1q35.2 duplication and phenotype correlation.
Mohamed, A M; El-Bassyouni, H T; El-Gerzawy, A M; Hammad, S A; Helmy, N A; Kamel, A K; Ismail, S I; Issa, M Y; Eid, O; Zaki, M S.
Afiliación
  • Mohamed AM; 1Division of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, 33-El-Bohooth St. Dokki, Cairo, 12311 Egypt.
  • El-Bassyouni HT; 2Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • El-Gerzawy AM; 1Division of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, 33-El-Bohooth St. Dokki, Cairo, 12311 Egypt.
  • Hammad SA; 1Division of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, 33-El-Bohooth St. Dokki, Cairo, 12311 Egypt.
  • Helmy NA; 1Division of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, 33-El-Bohooth St. Dokki, Cairo, 12311 Egypt.
  • Kamel AK; 1Division of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, 33-El-Bohooth St. Dokki, Cairo, 12311 Egypt.
  • Ismail SI; 2Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • Issa MY; 2Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
  • Eid O; 1Division of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, 33-El-Bohooth St. Dokki, Cairo, 12311 Egypt.
  • Zaki MS; 2Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.
Mol Cytogenet ; 11: 57, 2018.
Article en En | MEDLINE | ID: mdl-30410579

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mol Cytogenet Año: 2018 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mol Cytogenet Año: 2018 Tipo del documento: Article