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ISSN: 1755-8166 中科院分区: 生物(3区) 开放获取

Molecular Cytogenetics

简称 MOL CYTOGENET ·ENGLAND ·年均收录 83 篇

1.4

最新影响因子

7.80%

自引率

较易

投稿难度

>12周，或约稿

审稿周期

影响因子趋势

近期发表

Unbalanced X;14 translocation leading to turner syndrome phenotype: a case report and review of literature 2026-09-10

Expanding the phenotypic spectrum of hunter–McAlpine syndrome: a new case of distal 5q duplication and review of the literature 2026-08-29

Marker chromosomes in 15 individuals: cytogenetic delineation and molecular findings from SNP array analysis in a subset of cases 2026-08-11

A novel homozygous GLB1 pathogenic variant identified in two cases of infantile GM1 gangliosidosis 2026-08-03

Using SNP microarray to distinguish mosaicism from chimerism in a phenotypically normal male newborn with prenatal 46,XX/46,XY karyotype 2026-07-03

Previously unreported translocation (14;15)(q32; q11.2) observed in B-cell acute lymphoblastic leukemia: a case report 2026-06-19

Clinical presentation and genotype-phenotype correlation of a novel pure duplication of 6p25.2–p22.3: a case report and literature review 2026-06-18

Identification of tubulin gene variants in patients with dandy-walker malformation: expanding the spectrum of tubulinopathies 2026-06-17

Molecular cytogenetics provides insights into heterochromatin composition and karyotypic evolution in species of the Plebeia group (Apidae: Meliponini) 2026-06-16

A fetus with paternal uniparental isodisomy of chromosome 3: genetic analysis and prenatal diagnosis following a positive NIPS with IUGR 2026-06-15

Combined optical genome mapping and cnv-seq identify complex Y-chromosome rearrangements and ectopy in 46,XX testicular disorder of sex development 2026-06-14

Chromosomal abnormalities and copy number variations in fetuses with ventriculomegaly: a multicenter retrospective study 2026-05-27

Optical genome mapping uncovers disease-defining variants in an adult T-lymphoblastic leukemia and impacts prognosis 2026-05-24

Prenatal diagnosis and genetic counseling of a paternally inherited chromosome 5p13.3p13.2 microduplication in a Chinese family 2026-05-17

A ten-year follow up case report on monochorionic dizygotic twins with confined blood chimerism of 47,XY,+21/46,XX 2026-04-28

Prenatal diagnosis, genetic analysis, and pregnancy outcomes of fetuses with mosaic isodicentric Y chromosomes 2026-04-27

Antenatal discovery of mosaic trisomy 14 in an early-onset malformative syndrome 2026-04-24

Disheveled associated activator of morphogenesis 2 variants may produce alport-like changes: a case report 2026-04-24

Prenatal diagnosis and follow-up of a child with mosaic tetrasomy 9p without obvious abnormal clinical manifestations 2026-04-15

Discrepant findings of prenatal diagnostics in a case of fetal partial trisomy 21 and fetoplacental mosaicism 2026-04-11

期刊信息

ISSN

1755-8166

期刊简称

MOL CYTOGENET

国家/地区

ENGLAND

中科院分区

生物(3区)

开放获取

Yes

研究领域

GENETICS & HEREDITY-

收录范围

Science Citation Index Expanded

详细类别

GENETICS & HEREDITY遗传学4区

投稿与主页

投稿链接杂志主页

分析服务

分析服务

联系地址

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