D. Stevenson

Molecular diagnosis in hereditary hemorrhagic telangiectasia: findings in a series tested simultaneously by sequencing and deletion/duplication analysis

P. Bayrak-Toydemir, J. McDonald, W. Wooderchak, 2011, Clinical genetics.

Clinical and molecular aspects of an informative family with neurofibromatosis type 1 and Noonan phenotype

D. Stevenson, J. Carey, D. Viskochil, 2006, Clinical genetics.

Factors associated with the time to complete clinical exome sequencing in a pediatric patient population.

Albee Y. Ling, D. Stevenson, Linbo Yu, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Calibration of 6q subtelomere deletions to define genotype/phenotype correlations

D. Waggoner, J. Chung, D. Eash, 2005, Clinical genetics.

Neural tube defects and atypical deletion on 22q11.2

A. Rope, B. Krock, C. Leoni, 2014, American journal of medical genetics. Part A.

Molecular confirmation of HRAS p.G12S in siblings with Costello syndrome

J. Carey, K. Gripp, E. Hopkins, 2011, American journal of medical genetics. Part A.

A new distal arthrogryposis syndrome characterized by plantar flexion contractures

M. Bamshad, D. Stevenson, K. Swoboda, 2006, American journal of medical genetics. Part A.

Copy Number Variation analysis in 98 individuals with PHACE syndrome

S. McWeeney, U. Broeckel, E. Worthey, 2012, The Journal of investigative dermatology.

Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure

E. Zackai, I. Krantz, N. Spinner, 2015, Genetics in Medicine.

Factors associated with the time to complete clinical exome sequencing in a pediatric patient population.

Albee Y. Ling, D. Stevenson, Linbo Yu, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.