Related Experiment Videos
Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25
American Journal of Human Genetics
|October 27, 1997
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
A splice site and copy number variant responsible for TTC25-related primary ciliary dyskinesia.
European journal of medical genetics·2021
Variations in radioiodine ablation: decision-making after total thyroidectomy.
European journal of nuclear medicine and molecular imaging·2019
[Somatostatin receptor PET/CT (SSTR-PET/CT)].
Nuklearmedizin. Nuclear medicine·2018
Axenfeld-Rieger syndrome.
Clinical genetics·2017
Pharmacokinetics of coadministration of levothyroxine sodium and alendronate sodium new effervescent formulation.
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2017
Shared genetic basis and structure of syndromic and normal facial variation.
American journal of human genetics·2026
The Gabriella Miller Kids First Data Resource for genomic research in pediatric cancer and congenital anomalies.
American journal of human genetics·2026
Shared inheritance reveals landscape of somatic and germline cancer risk in TP53.
American journal of human genetics·2026
Examining gaps in institutional policies for clinical genomic data sharing: A cross-jurisdictional study.
American journal of human genetics·2026
Anthropometric and cardio-metabolic trait variation and genetic associations in sub-Saharan Africa.
American journal of human genetics·2026
Systematic and proactive evaluation of AIRE missense variant effects.
American journal of human genetics·2026
Triple carbapenemase-producing Klebsiella pneumoniae ST6668 resistant to novel β-lactam/β-lactamase inhibitor combinations and cefiderocol, Northern Italy, 2025.
International journal of antimicrobial agents·2026