Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Problems of genetic counseling in the presence of supernumerary marker chromosomes (case reports and a review of publications).

Folia medica - 1 Jan 1990

Stefanova M, Valkova G, Krustev T, Shishkova N

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child, Preschool
Share to Chromosome Aberrations
Share to Genetic Counseling
Share to Genetic Markers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant

Share to Infant, Newborn

Share to Pedigree

Share to Phenotype

Source

Identifiers

PMID: 2103915

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Problems of genetic counseling in the presence of supernumerary marker chromosomes (case reports and a review of publications).PMID 2103915Read ↗

Marker chromosomes.Semantic proximity Read ↗

Characterisation of supernumerary chromosomal markers: a study of 13 cases.Semantic proximity Read ↗

Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature.Semantic proximity Read ↗

Prenatal diagnosis of a small chromosome 2-derived supernumerary marker, and review of the reported cases.Semantic proximity Read ↗

[Cytogenetic and molecular genetic analysis of a case with mosaic marker chromosomes].Semantic proximity Read ↗

Derivative Complex Small Supernumerary Marker Chromosomes (sSMC) Involving Chromosome 2 and 15. A Novel Report.Semantic proximity Read ↗

Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: cooperative study of 19 Italian laboratories.Semantic proximity Read ↗

Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnosticsSemantic proximity Read ↗

Supernumerary marker chromosomes management in prenatal diagnosisSemantic proximity Read ↗

Misleading variant chromosome 12 in prenatal diagnosis.Semantic proximity Read ↗

Chromosome abnormalities in human beingsSemantic proximity Read ↗

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

⌁Select a neighboring publication to make it the new centre.