BIOMAT Database Logo BIOMAT Database Logo

A chromosomal abnormality (21q-) in primary thrombocytosis. 1979

P Petit, and H Van den Berghe

A patient with thrombocytosis was found to present an acquired deletion of the long arm of chrosome 21 (21q-). A similar observation reported in the literature is hereby confirmed.

UI MeSH Term Description Entries
D002872 Chromosome Deletion Actual loss of portion of a chromosome. Monosomy, Partial,Partial Monosomy,Deletion, Chromosome,Deletions, Chromosome,Monosomies, Partial,Partial Monosomies
D002904 Chromosomes, Human, 21-22 and Y The short, acrocentric human chromosomes, called group G in the human chromosome classification. This group consists of chromosome pairs 21 and 22 and the Y chromosome. Chromosomes G,Group G Chromosomes,Chromosomes, Human, 21 22,Chromosomes, Human, 21-22,Chromosome, Group G,Chromosomes, Group G,Group G Chromosome
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000368 Aged A person 65 years of age or older. For a person older than 79 years, AGED, 80 AND OVER is available. Elderly
D013922 Thrombocytosis Increased numbers of platelets in the peripheral blood. (Dorland, 27th ed) Thrombocythemia,Thrombocythemias,Thrombocytoses

Related Publications

P Petit, and H Van den Berghe
A chromosomal abnormality in primary thrombocythemia.
June 1978, The New England journal of medicine,
P Petit, and H Van den Berghe
Is chromosome 10 a primary chromosomal abnormality in endometrial adenocarcinoma?
July 1990, Cancer genetics and cytogenetics,
P Petit, and H Van den Berghe
Subtelomeric trisomy 21q: a new benign chromosomal variant.
January 2007, European journal of medical genetics,
P Petit, and H Van den Berghe
Partial trisomy 1q. A nonrandom primary chromosomal abnormality in myelodysplastic syndromes?
October 1991, Cancer genetics and cytogenetics,
P Petit, and H Van den Berghe
[Chromosomal abnormality].
September 1969, Nihon rinsho. Japanese journal of clinical medicine,
P Petit, and H Van den Berghe
XXXY chromosomal abnormality in a child.
January 1970, California medicine,
P Petit, and H Van den Berghe
A specific chromosomal abnormality in rhabdomyosarcoma.
January 1987, Cytogenetics and cell genetics,
P Petit, and H Van den Berghe
[Chromosomal abnormality in leukemia].
February 1989, Rinsho byori. The Japanese journal of clinical pathology,
P Petit, and H Van den Berghe
[Analyzing chromosomal abnormality in primary esophageal cancer by comparative genomic hybridization].
February 2007, Ai zheng = Aizheng = Chinese journal of cancer,
P Petit, and H Van den Berghe
A chromosomal abnormality in acute myeloblastic leukemia.
January 1963, The New England journal of medicine,
Copied contents to your clipboard!