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Article

A phenotypical male infant with 46,X,der(Y)t(X;Y)(?;p11) de novo.

Annales de genetique - 1 Jan 1997

Govaerts L C, Draaisma J M, vd Blij-Philipsen M, Smeets D F

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Share to In Situ Hybridization, Fluorescence
Share to Infant, Newborn
Share to Karyotyping
Share to Phenotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Sex Chromosome Aberrations

Share to Translocation, Genetic

Share to Y Chromosome

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Identifiers

PMID: 9150849

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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A phenotypical male infant with 46,X,der(Y)t(X;Y)(?;p11) de novo.PMID 9150849Read ↗

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Prenatal diagnosis and prenatal imaging of a <i>de novo</i> 46,X,der(Y)t(X;Y)(p22.13;q11.23) leading to functional disomy for the distal end of the X chromosome short arm from Xp22.13 in a phenotypically male fetus with posterior fossa abnormalitiesSemantic proximity Read ↗

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Developmental disability and hypomelanosis of Ito in a female with 7.3 Mb de novo duplication of Xp11.3-p11.4 and random X inactivation.Semantic proximity Read ↗

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Balloon pulmonary valvuloplasty for valvular pulmonary stenosis in double outlet right ventricle incriminating 46,X,der(X)t(X;3)(q28;q13.2)mat in an infant.Semantic proximity Read ↗

Unusual clinical syndrome in a boy with 45,X/46,XY mosaicism.Semantic proximity Read ↗

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