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

BACKGROUND: A prospective study using array CGH in children with Syndromic microcephaly from a tertiary pediatric healthcare centre in India. AIM: To identify the copy number variations causative of microcephaly detected through chromosomal array CGH. PATIENTS AND METHODS: Of the 60 patients, 33 (55...

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Detalles Bibliográficos
Autores principales: Goyal, Manisha, Faruq, Mohammed, Gupta, Ashok, Shrivastava, Divya, Shamim, Uzma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996492/
https://www.ncbi.nlm.nih.gov/pubmed/36911451
http://dx.doi.org/10.4103/aian.aian_202_22

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996492/
https://www.ncbi.nlm.nih.gov/pubmed/36911451
http://dx.doi.org/10.4103/aian.aian_202_22

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