Trisomy 21 mosaicism in two successive generations in a family

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Cleaved high-molecular-weight kininogen and its domain 5 inhibit migration and invasion of human prostate cancer cells through the epidermal growth factor receptor pathway.

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Novel ring chromosome composed of X- and Y-derived material in a girl with manifestations of Ullrich-Turner syndrome.

American journal of medical genetics·2000

Baboon/human homologies examined by spectral karyotyping (SKY): a visual comparison.

Cytogenetics and cell genetics·1998

Investigational vaccine for Escherichia coli O157: phase 1 study of O157 O-specific polysaccharide-Pseudomonas aeruginosa recombinant exoprotein A conjugates in adults.

The Journal of infectious diseases·1998

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Journal of medicinal chemistry·1997

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Journal of medical genetics·2026

Risk of breast cancer after ovarian cancer in germline BRCA1/2 heterozygotes.

Journal of medical genetics·2026

Rapid minigene workflow for functional reclassification of splicing variants in hereditary cancer diagnostics.

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Childhood-onset neurodegeneration and brain atrophy: defining UBTF-related developmental regression and progressive ataxia.

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BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Journal of medical genetics·2026

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Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

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Molecular carcinogenesis·2026

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iScience·2026

Single-nuclei RNA sequencing reveals obesity-associated rewiring of estrogen signaling in endometrioid adenocarcinoma.

iScience·2026

Changes in postoperative symptom communities and network structure in patients with oral squamous cell carcinoma: A four-time-point study.

Asia-Pacific journal of oncology nursing·2026

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Trisomy 21 mosaicism in two successive generations in a family

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Milestones in the development and implementation of FRET-based sensors of intracellular signals: A biological perspective of the history of FRET.

Cleaved high-molecular-weight kininogen and its domain 5 inhibit migration and invasion of human prostate cancer cells through the epidermal growth factor receptor pathway.

Novel ring chromosome composed of X- and Y-derived material in a girl with manifestations of Ullrich-Turner syndrome.

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Childhood-onset neurodegeneration and brain atrophy: defining UBTF-related developmental regression and progressive ataxia.

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Trisomy 21 mosaicism in two successive generations in a family

Abstract:

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