(Q41527352)

2 October 2017

1 reference

title

Monosomy 7 and 7q--associated with myeloid malignancy (English)

1 reference

2 October 2017

Johnson E

1

1 reference

PubMed ID

9218106

2 October 2017

Cotter FE

series ordinal

2

1 reference

2 October 2017

1 March 1997

1 reference

2 October 2017

1 reference

2 October 2017

11

1 reference

2 October 2017

46-55

1 reference

2 October 2017

1

1 reference

Recurrent chromosomal defects are found in most patients with acute nonlymphocytic leukemia

2 October 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

A summary of 7q interstitial deletions and exclusion mapping of the gene for beta-glucuronidase

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Myelodysplastic syndromes in childhood: three case reports

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Juvenile monosomy 7 syndrome: evidence that the disease originates in a pluripotent hemopoietic stem cell

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Simple monosomy 7 and myelodysplastic syndrome in thirteen patients without previous cytostatic treatment

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Monosomy 7 in childhood: a myeloproliferative disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Myelodysplastic syndromes in childhood: a population based study of nine cases

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Primary myelodysplastic syndrome in children: the clinical experience in 33 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Monosomy 7 syndrome. Clinical heterogeneity in children and adolescents

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Chromosome pattern, occupation, and clinical features in patients with acute nonlymphocytic leukemia.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Chromosome changes in acute leukaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: further evidence for characteristic abnormalities of chromosomes no. 5 and 7

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Monosomy 7 in multilineage and acute lymphoblastic leukaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Clonality of cell populations in refractory anaemia using combined approach of gene loss and X-linked restriction fragment length polymorphism-methylation analyses

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Fluorescence in situ hybridisation studies to characterise complete and partial monosomy 7 in myeloid disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Chromosome 7 long-arm deletions in myeloid disorders: terminal DNA sequences are commonly conserved and breakpoints vary

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Translocation 1;7 in dyshematopoiesis: possibly induced with a nonrandom geographic distribution

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Translocation 1;7 in hematologic disorders: a brief review of 22 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

t(1;7)(p36;q32): a new recurring abnormality in primary myelodysplastic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Survival of patients with t(1;7)(p11;p11). Report of two cases and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Translocation 1;7 in preleukemic states

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Deletions of the long arm of chromosome 7 in myeloid disorders: loss of band 7q32 implies worst prognosis

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Refined chromosome study helps define prognostic subgroups in most patients with primary myelodysplastic syndrome and acute myelogenous leukaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Hematologic, clinical, and cytogenetic analysis in 109 patients with primary myelodysplastic syndrome. Prognostic significance of morphology and chromosome findings

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Erythropoiesis during an erythroblastic phase of chronic myeloproliferative disorder associated with monosomy 7

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Monosomy 7 and multipotential stem cell transformation.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Bone marrow dysfunctions preceding acute leukemia in children: A clinical study

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Preleukemia in children

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Cytogenetics of childhood preleukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Age- and gender-related heterogeneity of cancer chromosome aberrations

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Proposals for the classification of the myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Subacute and chronic myelomonocytic leukemia in children (juvenile CML). Clinical and hematologic observations, and identification of prognostic factors

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Childhood monosomy 7 revisited.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Morphologic, immunologic and cytogenetic studies in acute myeloid leukemia following occupational exposure to pesticides and organic solvents.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Occupational history and involvement of chromosomes 5 and 7 in acute nonlymphocytic leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Myeloid neoplasia in children treated for solid tumours.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Evolution of acquired severe aplastic anaemia to myelodysplasia and subsequent leukaemia in adults

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Myelodysplasia and acute myeloid leukaemia in cases of aplastic anaemia and congenital neutropenia following G-CSF administration

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Myelodysplasia and leukemia after treatment of aplastic anemia with G-CSF

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Rate-limiting steps: The genetics of pediatric cancers

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Infantile genetic agranulocytosis. A review with presentation of ten new cases

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Effects of recombinant human granulocyte colony-stimulating factor on neutropenia in patients with congenital agranulocytosis

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Mutations in the gene for the granulocyte colony-stimulating-factor receptor in patients with acute myeloid leukemia preceded by severe congenital neutropenia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Transformation of congenital neutropenia into monosomy 7 and acute nonlymphoblastic leukemia in a child treated with granulocyte colony-stimulating factor

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Terminal acute myelogenous leukemia in a patient with congenital agranulocytosis

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

THE SYNDROME OF PANCREATIC INSUFFICIENCY AND BONE MARROW DYSFUNCTION.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

The occurrence of leukemia in patients with the Shwachman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

NF1: a prevalent cause of tumorigenesis in human cancers?

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Neurofibromatosis and childhood leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Neurofibromatosis and childhood leukaemia/lymphoma: a population-based UKCCSG study

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Possible co-existence of RAS activation and monosomy 7 in the leukaemic transformation of myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in haematopoietic cells

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Leukemia and preleukemia in Fanconi anemia patients. A review of the literature and report of the International Fanconi Anemia Registry

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Chromosome abnormalities in bone marrow of Fanconi anemia patients

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Chromosome clues to acute leukemia in Down's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Chromosome 7 abnormalities in children with Down syndrome and preleukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Myelodysplasia and acute megakaryoblastic leukemia in Down's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Childhood bone marrow monosomy 7 syndrome: a familial disorder?

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Myelodysplasia and leukemia syndrome with monosomy 7: a genetic perspective.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Familial acute myelogenous leukemia with associated C-monosomy in two affected members

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Familial myelodysplasia: progressive disease associated with emergency of monosomy 7

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Familial leukemia and aplastic anemia associated with monosomy 7

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Familial bone marrow monosomy 7. Evidence that the predisposing locus is not on the long arm of chromosome 7.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monosomy 7.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Possible evidence for genomic imprinting in childhood acute myeloblastic leukaemia associated with monosomy for chromosome 7

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Allogeneic Marrow Transplantation in the Treatment of Preleukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Chromosome 7 long arm deletion breakpoints in preleukemia: mapping by pulsed field gel electrophoresis

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Molecular characterization of the 7q deletion in myeloid disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Molecular evidence that childhood monosomy 7 syndrome is distinct from juvenile chronic myelogenous leukemia and other childhood myeloproliferative disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Comparison of cytogenetic and restriction fragment length polymorphism analyses for the detection of loss of chromosome material in clonal hemopoietic disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Comparison between interphase and metaphase cytogenetics in detecting chromosome 7 defects in hematological neoplasias

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Detection of monosomy 7 in interphase cells of patients with myeloid disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Deletion of the acetylcholinesterase locus at 7q22 associated with myelodysplastic syndromes (MDS) and acute myeloid leukaemia (AML).

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Chromosomal assignment of the human erythropoietin gene and its DNA polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Apoptosis regulatory gene NEDD2 maps to human chromosome segment 7q34-35, a region frequently affected in haematological neoplasms

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Nonradioactive in situ hybridisation of the translocation t(1;7) in myeloid malignancies

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Fluorescence in situ hybridization analysis of whole-arm 7;12 translocations in hematologic malignancies

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

One FISH, two FISH, red FISH, blue FISH.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

Human haploinsufficiency — one for sorrow, two for joy

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2897%2990006-0

7 January 2021

10.1016/S0268-960X(97)90006-0

Identifiers

DOI

1 reference

2 October 2017

1 reference

PubMed ID

9218106