C. Henkle

发表

Clear cell sarcoma case report: complex karyotype including t(12;22) in primary and metastatic tumor.

C. Griffin, C. Henkle, A. Hawkins, 2004, Cancer genetics and cytogenetics.

Advances in Brief Recurrent Involvement of 2 p 23 in Inflammatory Myofibroblastic Tumors

C. Griffin, E. Perlman, C. Henkle, 1999 .

Trisomy 5 and trisomy 7 are nonrandom aberrations in pigmented villonodular synovitis: Confirmation of trisomy 7 in uncultured cells

J. Fletcher, C. Morton, A. Rosenberg, 1992, Genes, chromosomes & cancer.

Partial trisomy 8 (trisomy 8q2106 leads to 8qter).

D. Perl, C. Henkle, D. Abuelo, 1977, Journal of medical genetics.

Recurrent involvement of 2p23 in inflammatory myofibroblastic tumors.

C. Griffin, E. Perlman, C. Henkle, 1999, Cancer research.

Induction of c-fos and c-myc mRNA by epidermal growth factor or calcium ionophore is cAMP dependent.

J. Campisi, R. Levine, C. Henkle, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Immunological and cytogenetic studies in two cases of B-cell acute lymphoblastic leukemia (Burkitt's type).

J. Griffin, R. Mayer, C. Henkle, 1983, Cancer genetics and cytogenetics.

marrow eosinophils in acute myelomonocytic leukemia A pericentric inversion of chromosome 16 is associated with dysplastic

C. Henkle, H. Weinstein, R. Tantravahi, 2011 .

A pericentric inversion of chromosome 16 is associated with dysplastic marrow eosinophils in acute myelomonocytic leukemia.

J. Griffin, C. Henkle, H. Weinstein, 1984, Blood.

Immortal clones of NM1 keratinocytes contain an isochromosome of the long arm of chromosome 8

C. Henkle, H. Baden, S. Phillips, 2007, In Vitro Cellular & Developmental Biology.

Sequential development of distinct clonal chromosome abnormalities in a patient with preleukaemia

C. Henkle, H. Weinstein, R. Tantravahi, 1985, British journal of haematology.