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Article

Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: further confirmation.

Prenatal diagnosis - 1 Feb 2000

Hand J L, Michels V V, Marinello M J, Ketterling R P, Jalal S M

Abstract excerpt

We describe two families in which an inherited interstitial deletion is present without apparent associated phenotypic abnormalities. The first deletion was discovered in a 19-year-old male with a previously diagnosed peroxisomal disorder. High-resolution chromosome analysis was interpreted as 46,XY,del(5)(p14.1p14.3). The patient's phenotypically normal mother had the same interstitial deletion. Chromosome 5p14...

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Identifiers

PMID: 10694687
DOI: 10.1002/(sici)1097-0223(200002)20:2<144::aid-pd770>3.0.co;2-9

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Source receipt: pubmed, retrieved 7 Sept 2026.

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