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A Rare Case of Trisomy 15pter-q21.2 Due to a De Novo Marker Chromosome
(WILEY-LISS, 2010)
Supernumerary marker chromosomes (sSMC) may or may not be associated with an abnormal phenotype, depending on the presence of euchromatin, on their chromosomal origin and whether they are inherited. Over 80% of sSMCs are ...
A Rare Case of Trisomy 15pter-q21.2 Due to a de Novo Marker Chromosome
(Wiley-Blackwell, 2010-03-01)
Supernumerary marker chromosomes (sSMC) may or may not be associated with an abnormal phenotype, depending on the presence of euchromatin, on their chromosomal origin and whether they are inherited. Over 80% of sSMCs are ...
A newborn with partial pure trisomy of chromosome 7q inherited from paternal balanced translocation with congenital anomalies. a mini review
(Somil Shah, 2018-04)
We report on a familial translocation t(3;7)(3q29::7q22) leading to pure trisomy 7q22 --> 7qter in a 21-days-old boy: 46,XY,der(3;7)(3pter--> 3q29::7q22--> 7pter). By conventional citogenetic techniques including fluorescence ...