Assignment of ZNF262 to human chromosome band 1p34→p32 by in situ hybridization

Cytogenetics and Cell Genetics

Volumn 85, Issue 3-4, 1999, Pages 306-307

  Sohal, J ^a   Chase, A ^a   Goldman, J M ^a   Cross, N C P ^a  

^a IMPERIAL COLLEGE SCHOOL OF MEDICINE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN PROTEIN;

ARTICLE; CHROMOSOME 1P; CHROMOSOME BANDING PATTERN; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; IN SITU HYBRIDIZATION; METAPHASE CHROMOSOME; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

BLOTTING, NORTHERN; CARRIER PROTEINS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LEUKEMIA, LYMPHOCYTIC, ACUTE;

EID: 0032789876     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

1. Aguiar RCT, Chase A, Coulthard S, Macdonald DH, Carapeti M, Reiter A, Sohal J, Lennard A, Goldman JM, Cross NC: Abnormalities of chromosome band 8p11 in leukaemia: two clinical syndromes can be distinguished on the basis of MOZ involvement. Blood 90:3130-3138 (1997).
2. Harrison C, Cuneo A, Johansson B: Ten novel 11q23 partner sites. Leukaemia 12:811-822 (1998).
3. Macdonald D, Aguiar RCT, Mason PJ, Goldman JM, Cross NCP: A new myeloproliferative disorder associated with chromosomal translocations involving 8p11: a review. Leukemia 9:1628-1630 (1995).
4. Reiter A, Sohal J, Kulkarni S, Chase A, Macdonald DHC, Aguiar RCT, Goncalves C, Hernandez JM, Jennings BA, Goldman JM, Cross NCP: Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome. Blood 92:1735-1742 (1998).
5. Smedley D, Hamoudi R, Clark J, Warren W, Abdul Rauf M, Somers G, Venter D, Fagan K, Cooper C, Shipley J: The t(8;13)(p11;q11-12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP. Hum Mol Genet 7:637-642 (1998).
6. Suyama M, Nagase T, Ohara, O: HUGE: a database for human large proteins identified by Kazusa cDNA sequencing project. Nucl Acids Res 27:338-339 (1999).
7. van der Maarel SM, Scholten IH, Huber I, Philippe C, Suijkerbuijk RF, Gilgenkrantz S, Kere J, Cremers FP, Ropers HH: Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq 13.1. Hum Mol Genet 5:887-897 (1996).