C. Lee

发表

Limitations of chromosome classification by multicolor karyotyping.

D. Gisselsson, J. Fletcher, C. Lee, 2001, American journal of human genetics.

Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy 14 and monosomy 21.

L. Holmes, C. Lee, C. Morton, 2001, American journal of medical genetics.

Array-based comparative genomic hybridization and copy number variation in cancer research

Charles Lee, Eun Kyung Cho, J. Freeman, 2006, Cytogenetic and Genome Research.

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F.

S. Schwartz, C. Lee, C. Morton, 2001, Human molecular genetics.

Impaired nonhomologous end-joining provokes soft tissue sarcomas harboring chromosomal translocations, amplifications, and deletions.

L. Chin, F. Alt, R. DePinho, 2001, Molecular cell.

Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): A possible locus for Fryns syndrome

P. Donahoe, L. Holmes, C. Lee, 2006, American journal of medical genetics. Part A.

Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization.

P. Donahoe, D. Tibboel, C. Lee, 2005, American journal of human genetics.

Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9.

Joe C. Adams, J. Aster, C. Lee, 2001, Human molecular genetics.

Prevalence and penetrance of ZFPM2 mutations and deletions causing congenital diaphragmatic hernia

K. Lage, P. Donahoe, A. Kashani, 2015, Clinical genetics.

Homozygosity for a FBN1 missense mutation causes a severe Marfan syndrome phenotype

C. Lee, A. Jelin, J. Hogue, 2013, Clinical genetics.

Comprehensive conventional and molecular cytogenetic characterization of B-CPAP, a human papillary thyroid carcinoma-derived cell line.

C. Lee, C. Morton, A. Fusco, 2004, Cancer genetics and cytogenetics.

Characterization of familial Waldenstrom's macroglobulinemia.

C. Lee, C. Morton, S. Treon, 2006, Annals of oncology : official journal of the European Society for Medical Oncology.

22q 13 Deletion Syndrome: A Genetic Basis For Neurobehavioral Disorders?

C. Lee, L. Jocelyn, A. Chudley, 1999, Genetics in Medicine.

Clinical picture: Multicolour karyotyping.

C. Lee, C. Morton, L. Wilkins-Haug, 2001, Lancet.