Evidence map›Paper›PMID 38041464›Full record

ArticleInternational journal of fertility & sterility2023

Study on The Pedigrees of Three Cases of Whole-Arm Translocation in Hainan China and Literature Review: A Retrospective Study.

C Hen Yunchun, Lin Yao, Zhao Zhengmin, Huang Xuning, Kong Changying, Liang Chongnan

Open access · greenAbstract readCase Reports
In one paragraph

Article in International journal of fertility & sterility, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 73% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

C Hen Yunchun *Department of Laboratory Medicine, Haikou Hospital of Traditional Chinese Medicine, Haikou, China.ORCID 0000-0002-6554-3204
Lin Yao *Pediatrics, The Third People's Hospital of Haikou City, Haikou, China.
Zhao ZhengminDepartment of Laboratory Medicine, Haikou Hospital of Traditional Chinese Medicine, Haikou, China.
Huang XuningDepartment of Ultrasound Medicine, Second Affiliated Hospital of Hainan Medical University, Haikou, China.
Kong ChangyingDepartment of Ultrasound Medicine, Second Affiliated Hospital of Hainan Medical University, Haikou, China.
Liang ChongnanDepartment of Laboratory Medicine, Haikou Hospital of Traditional Chinese Medicine, Haikou, China. Email: kjk36633837@163.com.
Hainan Medical University · CNHainan Provincial Hospital of Traditional Chinese Medicine · CNHaikou City People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, in order to promote chromosome abnormality carriers eugenics, three patients with adverse pregnancy histories were examined by cytogenetics and their pedigrees further analyzed. In this retrospective study, approximately anticoagulant peripheral venous blood from the patients was collected for peripheral blood cell culture and chromosome analysis. Karyotypes were analyzed in the BEIONMED karyotype analysis system. The karyotypes of the three probands were all whole-arm translocations (WATs): case 1 (DatabaseNo.3591): 46, XY, t (7; 13) (p10; p10) dn, two years of marriage in which the spouse did not have pregnancy, with azoospermia; case 2 (Database No.3809): 46, XY, t(12; 17) (p10; q10), three spontaneous abortions within three years of marriage; case 3 (Database No.4914) 46, XX, t(2;6) (p10; q10) mat, 21ps+pat, a year of marriage without pregnancy. When the parents are carriers of WAT, the family should be considered to have a high reproductive risk, increasing the risk of producing offspring with chromosomal abnormalities. Three kinds of human chromosomal aberration karyotypes were reported for the first time providing an important basis for studying the occurrence and clinical consultation of chromosomal diseases.

Indexed as

Case ReportChromosomesGenetic CounselingWhole-Arm Translocation

Identifiers

PMID38041464
PMCPMC10692743
OpenAlexW4389279364

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.