J. Shields

发表

Phenotypically distinct subtypes of psychosis accompany novel or rare variants in four different signaling genes

R. Goetz, D. Malaspina, M. Chao, 2016, EBioMedicine.

A deleted chromosome no. 13 in human retinoblastoma cells: relevance to tumorigenesis.

W. W. Nichols, R. Hill, A. Meadows, 1981, Cancer genetics and cytogenetics.

Concordance between parental origin of chromosome 13q loss and chromosome 6p duplication in sporadic retinoblastoma.

L. Strong, P. Jones, A. Naumova, 1994, American journal of human genetics.

Human esterase D gene: complete cDNA sequence, genomic structure, and application in the genetic diagnosis of human retinoblastoma

L. Donoso, E. Y. Lee, Wen-Hwa Lee, 1988, Human Genetics.

Genetic associations of the interleukin locus at 1q32.1 with clinical outcomes of cutaneous melanoma

T. Kirchhoff, D. Polsky, I. Osman, 2015, Journal of Medical Genetics.

Abnormalities of chromosome #13 in retinoblastomas from individuals with normal constitutional karyotypes.

A. Meadows, F. Gilbert, G. Balaban, 1982, Cancer genetics and cytogenetics.

Genetic variation in immunomodulatory genes as markers of melanoma recurrence-free and overall survival.

T. Kirchhoff, I. Osman, A. Pavlick, 2013 .

Retinoblastoma. Immunohistochemistry and cell differentiation.

D. Friendly, L. Donoso, G. Chader, 1987, Ophthalmology.