Further Insights into Developmental Brain Malformations and Leukoencephalopathy Associated with 6p25.3 Deletion.

Eid, Maha; Eid, Ola; Hegazy, Ibrahim; Girgis, Marian; Mohamed, Amal; Abdel-Salam, Ghada M H

Eid, Maha; Eid, Ola; Hegazy, Ibrahim; Girgis, Marian; Mohamed, Amal; Abdel-Salam, Ghada M H.

Afiliação

Eid M; Human Cytogenetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
Eid O; Human Cytogenetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
Hegazy I; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
Girgis M; Pediatric Department, Faculty of Medicine, Cairo University, Cairo, Egypt.
Mohamed A; Human Cytogenetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
Abdel-Salam GMH; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

Neuropediatrics ; 51(1): 76-82, 2020 02.

Article em En | MEDLINE | ID: mdl-31634935

Assuntos

Cromossomos Humanos Par 6/genética; Deleção de Genes; Cardiopatias Congênitas/genética; Leucoencefalopatias/genética; Lisencefalia/genética; Polimicrogiria/genética; Duplicação Cromossômica/genética; Cromossomos Humanos Par 7/genética; Feminino; Humanos; Lactente

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 6 / Deleção de Genes / Lisencefalia / Leucoencefalopatias / Polimicrogiria / Cardiopatias Congênitas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Infant Idioma: En Revista: Neuropediatrics Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Egito

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