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Literature DB >> 4128073

Letter: Deletions of chromosome 7 in haematological disorders.

J D Rowley.

Abstract

Entities: Disease

Mesh：

Year: 1973 PMID： 4128073 DOI： 10.1016/s0140-6736(73)93347-3

Source DB: PubMed Journal: Lancet ISSN： 0140-6736 Impact factor: 79.321

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7 in total

1. Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 cases.

Authors: F Pasquali; P Bernasconi; R Casalone; M Fraccaro; C Bernasconi; M Lazzarino; E Morra; E P Alessandrino; M A Marchi; R Sanger
Journal: Hum Genet Date: 1982 Impact factor: 4.132

2. Four families with immunodeficiency and chromosome abnormalities.

Authors: D C Candy; A R Hayward; D T Hughes; L Layward; J F Soothill
Journal: Arch Dis Child Date: 1979-07 Impact factor: 3.791

3. CUX1 is a haploinsufficient tumor suppressor gene on chromosome 7 frequently inactivated in acute myeloid leukemia.

Authors: Megan E McNerney; Christopher D Brown; Xiaoyue Wang; Elizabeth T Bartom; Subhradip Karmakar; Chaitanya Bandlamudi; Shan Yu; Jinkyung Ko; Barry P Sandall; Thomas Stricker; John Anastasi; Robert L Grossman; John M Cunningham; Michelle M Le Beau; Kevin P White
Journal: Blood Date: 2012-12-03 Impact factor: 22.113

Letter: Deletions of chromosome 7 in haematological disorders.

1. Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 cases.

2. Four families with immunodeficiency and chromosome abnormalities.

3. CUX1 is a haploinsufficient tumor suppressor gene on chromosome 7 frequently inactivated in acute myeloid leukemia.

4. Editorial: Chromosomes and human neoplasms. Achievements using new staining techniques.

5. Nonrandom chromosomal abnormalities in hematologic disorders of man.

6. Somatic rearrangement of chromosome 14 in human lymphocytes.

7. Noncoding RNAs and Cancer.