Ade novo X; 3 translocation in Rett syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference20 articles.
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4. (1986): Rett syndrome-search for genetic markers. Am J Med Genet (Suppl 1): 377-382.
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4. Phenotypic variability in two infants sharing the same MECP2 mutation: evidence of chromosomal rearrangements and high sister-chromatid exchange levels in Rett syndrome;Acta Neurologica Belgica;2016-07-05
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