Molecular Biology
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8 july 2020 21:32:01 |
| Prenatal diagnosis of rearrangements in the fetal 22q11.2 region (Molecular Cytogenetics) |
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Tweet 22q11.2 deletion syndrome (22q11.2DS) and 22q11.2 duplication syndrome (22q11.2DupS) are the most common copy number variations in humans. The clinical phenotypes of these two syndromes are variable, and there... |
| 334 viewsCategory: Biotechnology, Genetics, Molecular Biology |
 Partial trisomy 4q and monosomy 5p inherited from a maternal translocationt(4;5)(q33; p15) in three adverse pregnancies (Molecular Cytogenetics)Genotype-phenotype correlation in 75 patients with small supernumerary marker chromosomes (Molecular Cytogenetics) 
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