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PubMed · 3879152

Partial monosomy 10p syndrome.

R Koenig·E Kessel·W Schoenberger
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Abstract

A newborn infant with monosomy 10p13 is reported. The clinical signs and symptoms of the present case are compared with those of previously described cases. Although there is no pathognomonic feature, a characteristic monosomy 10p syndrome is recognizable.

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Abnormalities, MultipleChromosome DeletionChromosomes, Human, 6-12 and XGrowth DisordersHumansInfant, NewbornKaryotypingMaleMonosomyCase ReportsJournal Article

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R Koenig, E Kessel, W Schoenberger. 1985. Partial monosomy 10p syndrome.. https://pubmed.ncbi.nlm.nih.gov/3879152/

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