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Clinical and Cytogenomic Characterization of De Novo 11p14.3-p15.5 Duplication Associated with 18q23 Deletion in an Egyptian Female Infant.
Afifi, Hanan H; El-Kamah, Ghada Y; Kamel, Alaa K; Abd Allah, Sally G; Hammad, Sayda; Sayed-Ahmed, Mohammed M; Hussein, Shymaa H; Mohamed, Amal M.
Afiliación
  • Afifi HH; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • El-Kamah GY; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Kamel AK; Human Cytogenetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Abd Allah SG; Human Cytogenetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Hammad S; Human Cytogenetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Sayed-Ahmed MM; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Hussein SH; Human Cytogenetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Mohamed AM; Human Cytogenetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
J Pediatr Genet ; 10(2): 131-138, 2021 Jun.
Article en En | MEDLINE | ID: mdl-33996184
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: J Pediatr Genet Año: 2021 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Alemania
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: J Pediatr Genet Año: 2021 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Alemania