Tetrasomy 13q mosaicism associated with phylloid hypomelanosis and precocious puberty
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32758/fullpdf
Reference19 articles.
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2. Molecular characterization of a human tyrosinase-related protein-2 cDNA. Patterns of expression in melanocytic cells;Bouchard;Eur J Biochem,1994
3. FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15:II. Review of the literature;Crolla;Am J Med Genet,1998
4. Congenital asymmetry associated with diploid-triploid mosaicism and large satellites;Ferrier;Lancet,1964
5. Mosaicism in human skin. Understanding the patterns and mechanisms;Happle;Arch Dermatol,1993
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1. Cytogenomic characterization of small supernumerary marker chromosomes in patients with pigmentary mosaicism;Frontiers in Genetics;2024-04-16
2. Prenatal identification of an inverted duplicated 13q marker chromosome with a neocentromere;Molecular Cytogenetics;2023-11-30
3. Nevi;Mosaicism in Human Skin;2022-11-24
4. Case Report: Prenatal Identification of a De Novo Mosaic Neocentric Marker Resulting in 13q31.1→qter Tetrasomy in a Mildly Affected Girl;Frontiers in Genetics;2022-07-19
5. Mosaic proximal trisomy 13q and regular trisomy 13 in a female patient with long survival: Involvement of an incomplete trisomic rescue and a chromothripsis event;Molecular Genetics & Genomic Medicine;2021-07-20
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