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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| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Medknow Publications
2022-01-01
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| coleção: | Annals of Indian Academy of Neurology |
| Assuntos: | |
| Acesso em linha: | http://www.annalsofian.org/article.asp?issn=0972-2327;year=2022;volume=25;issue=6;spage=1067;epage=1074;aulast=Goyal |
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