Partial trisomy of 7q resulting from a familial translocation

High repetition-rate dual-channel X-ray spectrometer for high-intensity laser-plasma experiments.

The Review of scientific instruments·2024

Flexible tape-drive target system for secondary high-intensity laser-driven sources.

The Review of scientific instruments·2023

Ultra-compact x-ray spectrometer for high-repetition-rate laser-plasma experiments.

The Review of scientific instruments·2022

Pregnancy outcomes in patients with psoriasis, psoriatic arthritis, or axial spondyloarthritis receiving ixekizumab.

The Journal of dermatological treatment·2021

Development of a deep learning based automated data analysis for step-filter x-ray spectrometers in support of high-repetition rate short-pulse laser-driven acceleration experiments.

The Review of scientific instruments·2021

Simulations of wavelength-multiplexed holography for single-shot spatiotemporal characterization of NIF's advanced radiographic capability (ARC) laser.

The Review of scientific instruments·2021

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Annales de genetique·2004

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Annales de genetique·2004

Large duplication 4q25-q34 with mild clinical effect.

Annales de genetique·2004

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Annales de genetique·2004

Partial trisomy 8q and partial monosomy 18p: a case report.

Annales de genetique·2004

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Annales de genetique·2004

Characterisation of the Novel HLA-A*32:207 Allele by Sequencing-Based Typing.

HLA·2026

Discovery of the Novel HLA-DQB1*05:386 Allele in a Brazilian Volunteer Donor.

HLA·2026

Identification of the Novel HLA-B*57:212 Allele by Next-Generation Sequencing.

HLA·2026

Characterisation of the Novel HLA-DRB3*01:127 Allele by Next-Generation Sequencing.

HLA·2026

Early-Onset TRNT1-Related SIFD Syndrome with an Additional Monoallelic C7 Variant: A Pediatric Case Report.

Diagnostics (Basel, Switzerland)·2026

Identification of the Novel HLA-DQB1*06:556 Allele by Next-Generation Sequencing.

HLA·2026

Related Experiment Videos

Partial trisomy of 7q resulting from a familial translocation

Related Concept Videos

High repetition-rate dual-channel X-ray spectrometer for high-intensity laser-plasma experiments.

Flexible tape-drive target system for secondary high-intensity laser-driven sources.

Ultra-compact x-ray spectrometer for high-repetition-rate laser-plasma experiments.

Pregnancy outcomes in patients with psoriasis, psoriatic arthritis, or axial spondyloarthritis receiving ixekizumab.

Development of a deep learning based automated data analysis for step-filter x-ray spectrometers in support of high-repetition rate short-pulse laser-driven acceleration experiments.

Simulations of wavelength-multiplexed holography for single-shot spatiotemporal characterization of NIF's advanced radiographic capability (ARC) laser.

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Large duplication 4q25-q34 with mild clinical effect.

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Partial trisomy 8q and partial monosomy 18p: a case report.

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Characterisation of the Novel HLA-A*32:207 Allele by Sequencing-Based Typing.

Discovery of the Novel HLA-DQB1*05:386 Allele in a Brazilian Volunteer Donor.

Identification of the Novel HLA-B*57:212 Allele by Next-Generation Sequencing.

Characterisation of the Novel HLA-DRB3*01:127 Allele by Next-Generation Sequencing.

Early-Onset TRNT1-Related SIFD Syndrome with an Additional Monoallelic C7 Variant: A Pediatric Case Report.

Identification of the Novel HLA-DQB1*06:556 Allele by Next-Generation Sequencing.

Related Experiment Videos

Partial trisomy of 7q resulting from a familial translocation

Related Concept Videos

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