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Article

Interstitial deletion of 16(q13q22) in a newborn resulting from a paternal insertional translocation.

Annales de genetique - 1 Jan 1991

Edelhoff S, Maier B, Trautmann U, Pfeiffer R A

Abstract excerpt

A dysmorphic newborn showed an interstitial deletion of the long arm of a chromosome 16 due to a balanced paternal insertional translocation 46,XY,ins(14;16)(q23;q13q22). The insertion was confirmed by chromosomal in situ suppression (CISS-) hybridization. Clinical features considered to be typical for a 16q- phenotype are demonstrated in this patient. Similar observations described in the literature are compared...

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Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 16
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 1746889

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Source receipt: pubmed, retrieved 7 Sept 2026.

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