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

Partial trisomy 1p due to paternal t(1;9) translocation in a family with recurrent miscarriages.

Fertility and sterility - 1 Jul 2006

Demirhan Osman, Tastemir Deniz

Abstract excerpt

OBJECTIVE: To report a new case with partial trisomy 1p due to paternal t(1;9) translocation in a family with recurrent miscarriages. DESIGN: Case report. SETTING: Faculty of Medicine, Cukurova University. PATIENT(S): A couple with recurrent miscarriages, an abnormal fetus, a newborn infant, paternal grandfather and grandmother. INTERVENTION(S): Chorionic villi sampling (CVS), amniocentesis, lymphocytic...

Read the complete abstract on PubMed

Topics

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

Share to Abortion, Habitual
Share to Chromosomes, Human, Pair 1
Share to Chromosomes, Human, Pair 9

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family

Share to Fathers

Share to Genetic Carrier Screening

Share to Translocation, Genetic

Share to Trisomy

Source

Identifiers

PMID: 16818035
DOI: 10.1016/j.fertnstert.2005.11.077

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

Partial trisomy 1p due to paternal t(1;9) translocation in a family with recurrent miscarriages.PMID 16818035Read ↗

Chromosomal abnormalities in couples with repeated fetal loss: An Indian retrospective studySemantic proximity Read ↗

Chromosomal aberrations in couples with pregnancy loss: A retrospective studySemantic proximity Read ↗

Parental balanced chromosomal rearrangement leading to major genomic imbalance and an autosomal trisomy resulting in consecutive pregnancy loss: a case report.Semantic proximity Read ↗

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

A high level of tetrasomy 9p mosaicism but no clinical manifestations other than moderate oligozoospermia with chromosomally balanced sperm: a case report.Semantic proximity Read ↗

[Probability rate of unbalanced offspring at birth and risk of unfavorable pregnancy outcomes in families of carriers of chromosomal reciprocal translocations involving chromosome 7].Semantic proximity Read ↗

[Analysis of a family with recurrent fetal copy number variations in 1p31.1].Semantic proximity Read ↗

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

The Analysis of Meiotic Segregation Patterns and Aneuploidy in the Spermatozoa of Father and Son With Translocation t(4;5)(p15.1;p12) and the Prediction of the Individual Probability Rate for Unbalanced Progeny at BirthSemantic proximity Read ↗

[Partial trisomy 1q due to maternal translocation].Semantic proximity Read ↗

Cytogenetic investigations in couples with repeated miscarriages and malformed children: report of a novel insertion.Semantic proximity Read ↗

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

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