Publication | Open Access
A new case of proximal 10q partial trisomy.
15
Citations
2
References
1991
Year
Mendelian DisorderMild Phenotypic AbnormalitiesCytogeneticsGenetic DisorderGeneticsChromosome 10Q11PathologyAneuploidyIdentical Chromosomal AberrationChromosomal RearrangementVariant InterpretationMedicineChromosome 9Proximal 10QClinical Genetics
We report on a girl with mild phenotypic abnormalities and duplication of chromosome 10q11----10q22. The similarities to two previously reported cases with an identical chromosomal aberration provide further support for the delineation of this entity as a specific, clinically recognisable syndrome.
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