A TECHNIQUE FOR SIMULTANEOUS DEMONSTRATION OF G BANDS AND SISTER CHROMATID EXCHANGESFONATSCH C.1979; CYTOGENET. CELL GENET.; CHE; DA. 1979; VOL. 23; NO 1-2; PP. 144-146; BIBL. 9 REF.Article

A SIMPLE METHOD TO DEMONSTRATE THE FRAGILE X CHROMOSOME IN FIBROBLASTSFONATSCH C.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 2; PP. 186; BIBL. 3 REF.Article

EFFECT OF NITROFURANTOIN ON MEIOSIS OF THE MALE MOUSE.FONATSCH C.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 3; PP. 345-351; BIBL. 1 P. 1/2Article

Cytogenetics of malignant lymphomasFONATSCH, C.Blut. 1988, Vol 57, Num 3, pp 101-109, issn 0006-5242Article

Cytogenetic markers in hematoproliferative disordersFONATSCH, C.Blut. 1985, Vol 51, Num 5, pp 315-328, issn 0006-5242Article

BALANCED RECIPROCAL WHOLE-ARM TRANSLOCATION T(1;19) IN THREE GENERATIONS.SCHOBER AM; FONATSCH C.1978; HUM. GENET.; DEU; DA. 1978; VOL. 42; NO 3; PP. 349-352; BIBL. 9 REF.Article

PARTIAL TRISOMY 4Q AND PARTIAL MONOSOMY 18Q AS CONSEQUENCE OF A PATERNAL BALANCED TRANSLOCATION T(4Q; 18Q+)FONATSCH C; FLATZ SD; HURTER P et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 25; NO 3; PP. 227-233; BIBL. 8REF.Article

PARTIAL TRISOMY 13 PLUS PARTIAL TRISOMY 49 DUE TO UNUSUAL SEGREGATION OF TRANSLOCATION CHROMOSOMESFONATSCH C; FLATZ SD; WEITZEL E et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 2; PP. 176-182; BIBL. 23 REF.Article

REPLICATION PATTERN IN XXY CELLS WITH FRA(X)FROSTER ISKENIUS U; SCHWINGER E; WEIGERT M et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 3; PP. 278-280; BIBL. 9 REF.Article

H-Y ANTIGEN IN MALE PATIENTS WITH X POLYSOMIESENGEL W; KLEMME B; PROBECK HD et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 2; PP. 110-112; BIBL. 13 REF.Article

TWO NEOPLASTIC CELL LINES WITH UNIQUE FEATURES DERIVED FROM HODGKIN'S DISEASESCHAADT M; DIEHL V; STEIN H et al.1980; INT. J. CANCER; ISSN 0020-7136; CHE; DA. 1980; VOL. 26; NO 6; PP. 723-731; BIBL. 2 P.Article

Cytogenetic peculiarities in chronic myelogenous leukemiaHILD, F; FONATSCH, C.Cancer genetics and cytogenetics. 1990, Vol 47, Num 2, pp 197-217, issn 0165-4608Article

A POSSIBLE CORRELATION BETWEEN THE DEGREE OF KARYOTYPE ABERRATIONS AND THE RATE OF SISTER CHROMATID EXCHANGES IN LYMPHOMA LINESFONATSCH C; SCHAADT M; KIRCHNER H et al.1980; INT. J. CANCER; ISSN 0020-7136; CHE; DA. 1980; VOL. 26; NO 6; PP. 749-756; BIBL. 27 REF.Article

INTRACRANIAL HETEROTRANSPLANTATION OF HUMAN HEMATOPOIETIC CELLS IN NUDE MICESCHAADT M; KIRCHNER H; FONATSCH C et al.1979; INTERNATION. J. CANCER; CHE; DA. 1979; VOL. 23; NO 6; PP. 751-761; ABS. FRE; BIBL. 2 P.Article

TRANSLOCATION T (8;22) IN PERIPHERAL LYMPHOCYTES AND ESTABLISHED LYMPHOID CELL LINES FROM A PATIENT WITH HODGKINS DISEASE FOLLOWED BY ACUTE LYMPHATIC LEUKEMIAFONATSCH C; BURRICHTER H; SCHAADT M et al.1982; INT. J. CANCER; ISSN 0020-7136; CHE; DA. 1982; VOL. 30; NO 3; PP. 321-327; BIBL. 2 P.Article

HODGKIN'S DISEASE: ESTABLISHMENT AND CHARACTERIZATION OF FOUR IN VITRO CELL LINESDIEHL V; KIRCHNER HH; SCHAADT M et al.1981; J. CANCER RES. CLIN. ONCOL.; ISSN 0171-5216; DEU; DA. 1981; VOL. 101; NO 1; PP. 111-124; BIBL. 26 REF.Conference Paper

Heterochromatin and nucleolus organizer regions in cells of patients with malignant and premalignant lymphatic diseasesSCHULZE, B; GOLINSKI, C; FONATSCH, C et al.Human genetics. 1984, Vol 67, Num 4, pp 391-395, issn 0340-6717Article

Illegitimate splicing of the NF1 gene in healthy individuals mimics mutation-induced splicing alterations in NF1 patientsWIMMER, K; ECKART, M; REHDER, H et al.Human genetics. 2000, Vol 106, Num 3, pp 311-313, issn 0340-6717Article

Mutational analysis of the tumor suppressor Smad2 in acute lymphoid and myeloid leukemiaWIESER, R; GRUBER, B; RIEDER, H et al.Leukemia. 1998, Vol 12, Num 7, pp 1114-1118, issn 0887-6924Article

Abnormalities of the short arm of chromosome 9: a nonrandom secondary aberration in Philadelphia chromosome-positive acute lymphoblastic leukemia (ALL)RIEDER, H; FONATSCH, C; FREUND, M et al.Cancer genetics and cytogenetics. 1991, Vol 53, Num 1, pp 139-142, issn 0165-4608, 4 p.Article

Translocation (6;9) (p23;q34) in smoldering leukemia and acute nonlymphocytic leukemiaFONATSCH, C; STOLLMANN, B; HOLLDACK, J et al.Cancer genetics and cytogenetics. 1987, Vol 26, Num 2, pp 363-368, issn 0165-4608Article

Assignment of the TCP1 locus to the long arm of human chromosome 6 by in situ hybridizationFONATSCH, C; GRADL, G; RAGOUSSIS, J et al.Cytogenetics and cell genetics. 1987, Vol 45, Num 2, pp 109-112, issn 0301-0171Article

A CORRELATED STUDY OF THE CYTOGENETIC EFFECT OF ISONIAZID (INH) ON CELL SYSTEMS OF MAMMALS AND MAN CONDUCTED BY THIRTEEN LABORATORIES.ROHRBORN G; MILTENBURGER HG; RADENBACH KL et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 42; NO 1; PP. 1-60; BIBL. DISSEM.Article

Assignment of the human Ki-67 gene (MKI67) to 10q25-qterFONATSCH, C; DUCHROW, M; RIEDER, H et al.Genomics (San Diego, Calif.). 1991, Vol 11, Num 2, pp 476-477, issn 0888-7543Article

Chromosomal in situ hybridization of a Hodgkin's disease-derived cell line (L540) using DNA probes for TCRA, TCRB, MET, and rRNAFONATSCH, C; GRADL, G; KOLBUS, U et al.Human genetics. 1990, Vol 84, Num 5, pp 427-434, issn 0340-6717Article