Publications:

Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype.

Plos One

Collins, Stephen C SC; Coffee, Brad B; Benke, Paul J PJ; Berry-Kravis, Elizabeth E; Gilbert, Fred F; Oostra, Ben B; Halley, Dicky D; Zwick, Michael E ME; Cutler, David J DJ; Warren, Stephen T ST

Publication Date: 2010-03-05

Variant appearance in text: rs29285

PubMed Link: 20221430

Variant Present in the following documents:

• Main text
• pone.0009476.pdf

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