Works matching IS 17558166 AND DT 2025 AND VI 18 AND IP 1

Results: 10

Optical genome mapping enhances cytogenetic analysis in recurrent miscarriage: confirmation of a suspected (1;10) chromosomal translocation.

Published in:

2025

By:

del Águila, María del Mar;
Bernal, Mónica;
Vílchez, José Ramón;
Romero, Bárbara;
Castilla, José Antonio;
Álvarez, Gemma;
Clavero, Ana;
Poyatos, Antonio;
Ruíz-Cabello, Francisco

Publication type:

Case Study

Epigenomic insights and computational advances in hematologic malignancies.

Published in:

Molecular Cytogenetics (17558166), 2025, v. 18, n. 1, p. 1, doi. 10.1186/s13039-025-00712-9

By:

Lauzon-Young, Carolyn;
Silva, Ananilia;
Sadikovic, Bekim

Publication type:

Article

Prenatal diagnosis and molecular cytogenetic analyses of a rare 15q21.3 and 16p11.2 microduplication family.

Published in:

Molecular Cytogenetics (17558166), 2025, v. 18, n. 1, p. 1, doi. 10.1186/s13039-025-00711-w

By:

Zhang, Fei;
Liao, Gaoqi;
Wen, Xin;
Zhang, Chengcheng

Publication type:

Article

Genomic landscape of childhood acute lymphoblastic leukemia in Malaysia: insights from array-CGH.

Published in:

Molecular Cytogenetics (17558166), 2025, v. 18, n. 1, p. 1, doi. 10.1186/s13039-025-00709-4

By:

Ismail, Azli;
Ahid, Fadly;
Moi, Wong Nyuk;
Kamaluddin, Nor Rizan;
Esa, Ezalia;
Yusoff, Yuslina Mat;
Seman, Zahidah Abu;
Mohammed, Muhammad Asyraff;
George, Elizabeth;
Isa, Asmida;
Zakaria, Zubaidah

Publication type:

Article

Machine learning-based identification of telomere-related gene signatures for prognosis and immunotherapy response in hepatocellular carcinoma.

Published in:

Molecular Cytogenetics (17558166), 2025, v. 18, n. 1, p. 1, doi. 10.1186/s13039-025-00705-8

By:

Lu, Zhengmei;
Chai, Xiaowei;
Li, Shibo

Publication type:

Article

Novel MSH6 exon 5–6 skipping variant in a Taiwanese family with Lynch syndrome: implications for genetic testing and cancer management.

Published in:

Molecular Cytogenetics (17558166), 2025, v. 18, n. 1, p. 1, doi. 10.1186/s13039-025-00708-5

By:

Wang, Ting-Yao;
Chen, Chao-Yu;
Chuang, Huei-Chieh;
Jiang, Yuan-Yuan;
Lung, Jrhau

Publication type:

Article

Whole genome uniparental isodisomy detected using single nucleotide polymorphism (SNP) microarray in molar pregnancy: a case report.

Published in:

2025

By:

Okonkwo, Onyinye O.;
Ortega, Veronica;
Kane, Sheila;
Aldrete, Galina;
Ramirez, Paulina;
Valente, Philip T.;
Velagaleti, Gopalrao V.N.

Publication type:

Case Study

Prevalence of CNVs on the X chromosome in patients with neurodevelopmental disorders.

Published in:

Molecular Cytogenetics (17558166), 2025, v. 18, n. 1, p. 1, doi. 10.1186/s13039-025-00703-w

By:

Tolmacheva, Ekaterina N.;
Kashevarova, Anna A.;
Fonova, Elizaveta A.;
Salyukova, Olga A.;
Seitova, Gulnara N.;
Nazarenko, Lyudmila P.;
Agafonova, Anna A.;
Minaycheva, Larisa I.;
Ravzhaeva, Ekaterina G.;
Petrova, Valeria V.;
Lopatkina, Maria E.;
Belyaeva, Elena O.;
Vovk, Svetlana L.;
Fedotov, Dmitry A.;
Vasilyeva, Oksana Y.;
Skryabin, Nikolay A.;
Lebedev, Igor N.

Publication type:

Article

Preparing high-quality chromosome spreads from Crocus species for karyotyping and FISH: High-quality chromosome spreads in Crocus: A. El-nagish et al.

Published in:

Molecular Cytogenetics (17558166), 2025, v. 18, n. 1, p. 1, doi. 10.1186/s13039-025-00706-7

By:

El-nagish, Abdullah;
Liedtke, Susan;
Breitenbach, Sarah;
Heitkam, Tony

Publication type:

Article

Phenotypic and genotypic insights into concurrent tertiary trisomy for 9p and 18p.

Published in:

2025

By:

Wright, Carter A.;
Scheuerle, Angela E.;
Wilson, Kathleen;
García, Rolando;
Koduru, Prasad

Publication type:

Case Study