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1.
Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously Mapped to Chromosome 10q23-q24.
PLoS One
; 11(6): e0157418, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-27309958
2.
Localisation Of The Usher Syndrome Type I Gene In The French Acadian Population Of Louisiana To Chromosome 11p14-p15.1 By Linkage and Haplotype Analysis.
Indian J Hum Genet
; 1995 Apr; 1(2): 93-103
Artículo
en Inglés
| IMSEAR | ID: sea-159769
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