The Clinical Diagnostic Utility of Array CGH in Children with Syndromic Microcephaly.

Goyal, Manisha; Faruq, Mohammed; Gupta, Ashok; Shrivastava, Divya; Shamim, Uzma

Goyal, Manisha; Faruq, Mohammed; Gupta, Ashok; Shrivastava, Divya; Shamim, Uzma.

Afiliação

Goyal M; Department of Pediatrics, Centre of Rare Diseases, SMS Medical College, Jaipur, Rajasthan, India.
Faruq M; CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Gupta A; Department of Pediatrics, Centre of Rare Diseases, SMS Medical College, Jaipur, Rajasthan, India.
Shrivastava D; School of Life Sciences, Jaipur National University, Jaipur, Rajasthan, India.
Shamim U; CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.

Ann Indian Acad Neurol ; 25(6): 1067-1074, 2022.

Article em En | MEDLINE | ID: mdl-36911451

Palavras-chave

Array CGH; chromosomal microdeletion; copy number variations; microcephaly; microduplication

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Idioma: En Revista: Ann Indian Acad Neurol Ano de publicação: 2022 Tipo de documento: Article

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