Related Experiment Videos
45,X/46,XY mosaicism and fragile X syndrome
Shannon L Banes1, Michael L Begleiter, Merlin G Butler
1Section of Medical Genetics and Molecular Medicine, Children's Mercy Hospitals and Clinics, Kansas City, Missouri 64108, USA.
American Journal of Medical Genetics. Part A
|December 12, 2002
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Influence of Molecular Genetic Classes on Behavior in Prader-Willi Syndrome.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics·2026
The clinical utility of functional testing in fibroblasts to diagnose primary mitochondrial disease.
medRxiv : the preprint server for health sciences·2026
Clinical Presentation, Genetics, and Laboratory Testing with Integrated Genetic Analysis of Molecular Mechanisms in Prader-Willi and Angelman Syndromes: A Review.
International journal of molecular sciences·2026
Integrated Genetic and Protein Mechanisms Underlying Glucagon-like Peptide-1 Receptor Agonists in Treating Diabetes Mellitus and Weight Loss.
Current issues in molecular biology·2026
Exome Sequencing Uncovers Phenotypic and Genotypic Heterogeneity in 196 Indian Families Evaluated for Autoinflammatory Disorders.
American journal of medical genetics. Part A·2026
The Evaluation of Molecular Genetics and Clinical Manifestations in Patients With LZTR1-Associated Noonan Syndrome: A Retrospective Chart Review and Review of Literature.
American journal of medical genetics. Part A·2026
Expanding the Genotypic and Phenotypic Spectrum of Vissers-Bodmer Syndrome.
American journal of medical genetics. Part A·2026
Clinical and Functional Characterization of Gain-of-Function ABL1 Variants Expands the Phenotypic Spectrum of CHDSKM.
American journal of medical genetics. Part A·2026
Expanding the Clinical and Genetic Spectrum of Schmid Metaphyseal Chondrodysplasia: A Seven-Patient Series Including a Rare Homozygous COL10A1 Case.
American journal of medical genetics. Part A·2026
Rapid Genomic Testing: A Study of Institutional Utilization and Outcomes.
American journal of medical genetics. Part A·2026
Reconstruction of a neglected extensor hallucis tendon rupture with an iliotibial band autologous graft: case report.
International journal of surgery case reports·2026
Allograft Reconstruction Technique for Chronic Pectoralis Major Tears.
JBJS essential surgical techniques·2026
Single-cell mechanodynamics: Probing cellular function through nanomotion and intracellular mechanics.
Current opinion in structural biology·2026