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Publications by Ryan N Traylor
Proximal Microdeletions and Microduplications of 1q21.1 Contribute to Variable Abnormal Phenotypes
European Journal of Human Genetics
Genetics
Microdeletion of 6q16.1 Encompassing EPHA7 in a Child With Mild Neurological Abnormalities and Dysmorphic Features: Case Report
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
Related publications
Microduplications of 22q11.2 Are Frequently Inherited and Are Associated With Variable Phenotypes
Genetics in Medicine
Medicine
Genetics
Neurodevelopmental Genetic Diseases Associated With Microdeletions and Microduplications of Chromosome 17p13.3
Frontiers in Genetics
Genetics
Molecular Medicine
Prenatal Diagnosis of Microdeletions or Microduplications in the Proximal, Central, and Distal Regions of Chromosome 22q11.2: Ultrasound Findings and Pregnancy Outcome
Frontiers in Genetics
Genetics
Molecular Medicine
Behavioral Abnormalities Are Common and Severe in Patients With Distal 22q11.2 Microdeletions and Microduplications
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Abnormal Sub-Pathways Competitively Regulated by lncRNAs Contribute to Postmenopausal Osteoporosis
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
Mp79-01 Do Abnormal Toileting Behaviors Contribute to Worse Urinary Symptoms in Women?
Journal of Urology
Urology
Chromosomal Loci 22q11.2, 15q13.3 and 1q21.1
Science-Business eXchange
Variable Expression of Subclinical Phenotypes Instead of Reduced Penetrance in Families With Mild Triphalangeal Thumb Phenotypes
Journal of Medical Genetics
Genetics
A Cascade Leading to Premature Aging Phenotypes Including Abnormal Tumor Profiles in Werner Syndrome (Review)
International Journal of Molecular Medicine
Medicine
Genetics
