C. Killoran

发表

Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations

A. Guttmacher, L. Biesecker, J. Graham, 2001, Human Genetics.

Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes : Robust Phenotype Prediction from the Type and Position of GLI 3 Mutations

E. Zackai, L. Biesecker, J. Graham, 2005 .

Two cases of compositae dermatitis exacerbated by moisturizer containing feverfew.

Glen H. Crawford, C. Killoran, A. Pedvis-Leftick, 2007, Dermatitis.

The receptor for activated C-kinase-I (RACK-I) anchors activated PKC-β on melanosomes

B. Gilchrest, Heng Wu, Hee‐Young Park, 2004, Journal of Cell Science.

Localized Darier's disease in a Blaschkoid distribution: Two cases of phenotypic mosaicism and a review of mosaic Darier's disease

E. A. Sanderson, C. Wilkel, C. Killoran, 2007, The Journal of dermatology.

Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeres

J. Flint, L. Gaunt, J. Clayton-Smith, 1999, Journal of medical genetics.

Detection of chromosomal aberrations by a whole-genome microsatellite screen.

L. Biesecker, Y. Ning, R. Pauli, 2000, American journal of human genetics.

Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.

E. Zackai, A. Guttmacher, M. Bamshad, 2005, American journal of human genetics.

Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer

D. Cooper, L. Biesecker, J. Johnston, 2003, Human Genetics.

Overlap of PIV syndrome, VACTERL and Pallister–Hall syndrome: clinical and molecular analysis

L. Biesecker, M. Abbott, L. Biesecker, 2000, Clinical genetics.