(Q41090966)

26 September 2017

title

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

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26 September 2017

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Shannon KM

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26 September 2017

Turhan AG

series ordinal

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26 September 2017

Rogers PC

series ordinal

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26 September 2017

Kan YW

series ordinal

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26 September 2017

publication date

1 September 1992

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26 September 2017

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26 September 2017

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26 September 2017

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26 September 2017

page(s)

121-125

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

26 September 2017

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Sequence homology shared by neurofibromatosis type-1 gene and IRA-1 and IRA-2 negative regulators of the RAS cyclic AMP pathway.

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7 January 2021

Exon duplication and triplication in the human T-cell receptor gamma constant region genes and RFLP in French, Lebanese, Tunisian, and black African populations

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7 January 2021

Childhood bone marrow monosomy 7 syndrome: a familial disorder?

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7 January 2021

Ataxia-pancytopenia and monosomy 7 syndrome

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7 January 2021

Juvenile chronic myelogenous leukemia

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7 January 2021

Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.

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7 January 2021

The cellular functions of small GTP-binding proteins

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Uniparental paternal disomy in a genetic cancer-predisposing syndrome

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7 January 2021

Functional inactivation of genes by dominant negative mutations

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7 January 2021

Unbalanced translocation (1;7) in childhood myelodysplasia

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7 January 2021

Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13

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7 January 2021

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

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7 January 2021

Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma

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7 January 2021

Twenty-five loci form a continuous linkage map of markers for human chromosome 7

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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

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7 January 2021

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

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7 January 2021

A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10

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7 January 2021

Deletion of genes on chromosome 1 in endocrine neoplasia

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7 January 2021

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

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7 January 2021

Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients

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7 January 2021

Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene

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7 January 2021

Genome imprinting, cellular mosaicism and carcinogenesis.

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Monosomy 7 in childhood: a myeloproliferative disorder

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7 January 2021

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

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7 January 2021

The neurofibromatosis type 1 gene encodes a protein related to GAP

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7 January 2021

10.1016/S0888-7543(05)80293-9

Identifiers

DOI

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26 September 2017

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