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1.
Low-pass whole genome sequencing is a reliable and cost-effective approach for copy number variant analysis in the clinical setting.
Ann Hum Genet
; 88(2): 113-125, 2024 03.
Article
in English
| MEDLINE | ID: mdl-37807935
2.
[Hereditary tylosis syndrome and esophagus cancer]. / Síndrome tilose hereditária e câncer de esôfago.
An Bras Dermatol
; 84(5): 527-9, 2009.
Article
in Portuguese
| MEDLINE | ID: mdl-20098858
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