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A unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary marker chromosome 7
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SciELO - Brasil - Cellular consequences of small supernumerary marker chromosome derived from chromosome 12: mosaicism in daughter and father Cellular consequences of small supernumerary marker chromosome derived from chromosome 12: mosaicism
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Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis - Figure f3 | Aging
Analysis of the small supernumerary marker chromosomes of the patient.... | Download Scientific Diagram
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Figure 3 | Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally
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Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome - ScienceDirect
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Small Supernumerary Marker Chromosomes (sSMC) : A Guide for Human Geneticists and Clinicians (Hardcover) - Walmart.com
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Figure 1.3 from Small supernumerary marker chromosomes (sSMC) : why do they break, where they break and how to distinguish harmful from harmless sSMC? | Semantic Scholar
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OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11 - ScienceDirect
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