Neurofibromatosis type 1: A model condition for the study of the molecular basis of variable expressivity in human disorders
Author:
Affiliation:
1. Department of Pediatrics, Division of Medical Genetics, University of Utah Health Science Center, Salt Lake City, UT 84132
Publisher
Wiley
Subject
Genetics (clinical)
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/%28SICI%291096-8628%2819990326%2989%3A1%3C7%3A%3AAID-AJMG4%3E3.0.CO%3B2-%23
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