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Article

Is there an abnormal phenotype associated with maternal isodisomy for chromosome 2 in the presence of two isochromosomes?

American journal of human genetics - 1 Aug 1997

Shaffer L G, McCaskill C, Egli C A, Baker J C, Johnston K M

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Share to Abnormalities, Multiple
Share to Chromosome Aberrations
Share to Chromosome Disorders
Share to Chromosomes, Human, Pair 2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Infant, Newborn

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Identifiers

PMID: 9311755
DOI: 10.1016/S0002-9297(07)64076-2
PMCID: PMC1715890

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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Is there an abnormal phenotype associated with maternal isodisomy for chromosome 2 in the presence of two isochromosomes?PMID 9311755Read ↗

Normal phenotype with maternal isodisomy in a female with two isochromosomes: i(2p) and i(2q)Semantic proximity Read ↗

Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan.Semantic proximity Read ↗

Uniparental isodisomy for paternal 2p and maternal 2q in a phenotypically normal female with two isochromosomes, i(2p) and i(2q).Semantic proximity Read ↗

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Complete isochromosome 5p in one fetus of a monochorionic twin pairSemantic proximity Read ↗

Isochromosome Xq in mosaicism with a cell line with two normal X-chromosomes: association with psychomotor retardation and neurological deficit.Semantic proximity Read ↗

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Changes in an inherited ring (22) due to meiotic recombination? Implications for genetic counseling.Semantic proximity Read ↗

Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18Semantic proximity Read ↗

[Prenatal diagnosis of a fetus with two small supernumerary marker chromosomes].Semantic proximity Read ↗

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