Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome

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Bibliografske podrobnosti
Main Authors: CATCHPOOLE, D., SMALLWOOD, A., JOYCE, J., MURRELL, A., LAM, W., TANG, T., MUNROE, D., REIK, W., SCHOFIELD, P., MAHER, E.
Format: Artigo
Jezik:Inglês
Izdano: BMJ Group 2000
Teme:
Letters to the Editor
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734547/
https://ncbi.nlm.nih.gov/pubmed/10777363
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.37.3.212
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