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

Reproductive follow-up of carriers of familial reciprocal balanced translocations involving chromosome 9 and comparison with predicted outcome.

Genetic counseling (Geneva, Switzerland) - 1 Jan 2000

Castorina P, Rodeschini O, Nocera G, Larizza L

Abstract excerpt

Reproductive follow-up of carriers of familial reciprocal balanced translocations involving chromosome 9 and comparison with predicted outcome: Chromosome 9 is commonly implicated in reciprocal translocations (rcp). Twenty-seven families segregating rcp involving chromosome 9 were selected with the aim of comparing the theoretical risk of Mental Retardation with Congenital Anomalies (MCA/MR) calculated according...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 9
Share to Cytogenetics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Follow-Up Studies

Share to Genetic Predisposition to Disease

Share to Heterozygote

Share to Karyotyping

Share to Reproductive History

Share to Translocation, Genetic

Source

Identifiers

PMID: 11043431

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Reproductive follow-up of carriers of familial reciprocal balanced translocations involving chromosome 9 and comparison with predicted outcome.PMID 11043431Read ↗

Reciprocal chromosome translocations involving short arm of chromosome 9 as a risk factor of unfavorable pregnancy outcomes after meiotic malsegregation 2:2Semantic proximity Read ↗

Pregnancy outcomes of reciprocal translocation carriers with two or more unfavorable pregnancy histories: before and after preimplantation genetic testingSemantic proximity Read ↗

Correlation of clinical phenotype with a pericentric inversion of chromosome 9 and genetic counseling.Semantic proximity Read ↗

Reproductive outcomes in individuals with chromosomal reciprocal translocationsSemantic proximity Read ↗

Pregnancy outcome in carriers of Robertsonian translocationsSemantic proximity Read ↗

Pericentric inversion of chromosome 9 in prenatal diagnosis and infertility.Semantic proximity Read ↗

Reproductive outcome and fetal karyotype of couples with recurrent miscarriages.Semantic proximity Read ↗

[Pedigree analysis of childless families of reciprocal chromosome translocation carriers].Semantic proximity Read ↗

Positive reproductive family history for spontaneous abortion: predictor for recurrent miscarriage in young couples.Semantic proximity Read ↗

Chromosomal Abnormalities in Couples with Reproductive DisordersSemantic proximity Read ↗

Hereditary chromosomal 9 inversion (p22q13) 9 as a cause for recurrent pregnancy loss: a case report.Semantic proximity Read ↗

Pericentric inversion 9--incidence and clinical significance.Semantic proximity Read ↗

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