Primary transcription map of the critical region of the 5q-syndrome.

Primary transcription map of the critical region of the 5q-syndrome.

Bibliographic Details
Main Authors:	Boultwood, J, Fidler, C, Soularue, P, Kostrzewa, M, Strickson, A, Jaju, R, Cotter, F, Jabs, E, Lovett, M, Muller, U, Auffray, C, Wainscoat, W
Format:	Journal article
Published:	1996

Similar Items

Novel genes mapping to the critical region of the 5q- syndrome.
by: Boultwood, J, et al.
Published: (1997)

Isolation and analysis of novel genes mapping to the critical region of the 5q-syndrome
by: Fidler, C, et al.
Published: (1998)

Transcription mapping of the 5q- syndrome critical region: cloning of two novel genes and sequencing, expression, and mapping of a further six novel cDNAs.
by: Boultwood, J, et al.
Published: (2000)

Isolation and analysis of novel candidate genes mapping to the critical region of the 5q-syndrome.
by: Boultwood, J, et al.
Published: (1999)

Physical mapping of the human ATX1 homologue (HAH1) to the critical region of the 5q- syndrome within 5q32, and immediately adjacent to the SPARC gene.
by: Boultwood, J, et al.
Published: (2000)

ISOLATION OF NOVEL CDNA CLONES MAPPING TO THE CRITICAL REGION OF THE 5Q-CHROMOSOME IN THE 5Q-SYNDROME
by: Boultwood, J, et al.
Published: (1994)

Narrowing and genomic annotation of the critical region of the 5q-syndrome.
by: Boultwood, J, et al.
Published: (2000)

Molecular cytogenetic delineation of the critical deleted region in the 5q- syndrome.
by: Jaju, R, et al.
Published: (1998)

The human POP2 gene: identification, sequencing, and mapping to the critical region of the 5q- syndrome.
by: Fidler, C, et al.
Published: (1999)

Narrowing the critical deleted region in the 5q-syndrome.
by: Jaju, R, et al.
Published: (1996)

Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome.
by: Boultwood, J, et al.
Published: (2002)

MOLECULAR MAPPING OF UNCHARACTERISTICALLY SMALL 5Q DELETIONS IN 2 PATIENTS WITH THE 5Q- SYNDROME - DELINEATION OF THE CRITICAL REGION ON 5Q AND IDENTIFICATION OF A 5Q- BREAKPOINT
by: Boultwood, J, et al.
Published: (1993)

Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q- syndrome: delineation of the critical region on 5q and identification of a 5q- breakpoint.
by: Boultwood, J, et al.
Published: (1994)

Mutation analysis of the SPARC gene in the 5q-syndrome.
by: Fidler, C, et al.
Published: (2000)

A novel gene is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood AML.
by: Jaju, R, et al.
Published: (2000)

MOLECULAR MAPPING OF THE 7Q-DELETION IN MYELOID DISORDERS
by: Lewis, S, et al.
Published: (1993)

MOLECULAR DELINEATION OF THE CRITICAL REGION OF THE 5Q-CHROMOSOME IN THE 5Q-SYNDROME
by: Boultwood, J, et al.
Published: (1993)

A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia.
by: Jaju, R, et al.
Published: (2001)

Molecular characterization of the 7q deletion in myeloid disorders.
by: Lewis, S, et al.
Published: (1996)

Lineage studies of 5q deletions using combined immunophenotyping and fish.
by: Jaju, R, et al.
Published: (1999)

Combined immunophenotyping and FISH for identification of cell lineages with the 5q-abnormality
by: Jaju, R, et al.
Published: (1999)

Combined immunophenotyping and FISH identifies the involvement of B-cells in 5q- syndrome.
by: Jaju, R, et al.
Published: (2000)

A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood AML.
by: Jaju, R, et al.
Published: (1998)

NRAS, FLT3 and TP53 mutations in patients with myelodysplastic syndrome and a del(5q).
by: Fidler, C, et al.
Published: (2004)

Integrated physical and transcript map of 5q31.3-qter.
by: Kostrzewa, M, et al.
Published: (1998)

The 5q- syndrome.
by: Giagounidis, A, et al.
Published: (2004)

The 5q-syndrome.
by: Boultwood, J, et al.
Published: (1994)

5q- syndrome.
by: Boultwood, J, et al.
Published: (2012)

Telomere length in myelodysplastic syndromes.
by: Boultwood, J, et al.
Published: (1995)

Whole chromosome painting and FISH with subtelomeric probes reveals cryptic chromosome rearrangements in del(5q) leukaemias: a UK Cancer Cytogenetic Group study
by: Kearney, L, et al.
Published: (1999)

Allelic loss of IRF1 in myelodysplasia and acute myeloid leukemia: retention of IRF1 on the 5q- chromosome in some patients with the 5q- syndrome.
by: Boultwood, J, et al.
Published: (1993)

A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood acute myeloid leukemia. The UK Cancer Cytogenetics Group (UKCCG)
by: Jaju, R, et al.
Published: (1999)

A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood acute myeloid leukemia. The UK Cancer Cytogenetics Group (UKCCG)
by: Jaju, R, et al.
Published: (1999)

Genome-wide analysis of copy number change and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density SNP arrays
by: Wang, L, et al.
Published: (2007)

Adherence to deferoxamine therapy: Heeding hippocrates and osler
by: Watkins, F, et al.
Published: (2004)

BRCA2 gene deletion is rare in chronic lymphocytic leukemia.
by: Pilozzi, E, et al.
Published: (1998)

Mutations in PTPN11 are rare in adult myelodysplastic syndromes and acute myeloid leukemia.
by: Watkins, F, et al.
Published: (2004)

Gene expression profiling in the myelodysplastic syndromes.
by: Pellagatti, A, et al.
Published: (2005)

Physical and transcriptional characterization of the commonly deleted region in del(9q) AML.
by: Daly, S, et al.
Published: (2001)

Advances in the 5q- syndrome.
by: Boultwood, J, et al.
Published: (2010)