BIOMAT Database Logo BIOMAT Database Logo

Trisomy for the short arm of chromosome No. 10. 1974

T W Hustinx, and B G Ter Haar, and J M Scheres, and F J Rutten

UI MeSH Term Description Entries
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D007621 Karyotyping Mapping of the KARYOTYPE of a cell. Karyotype Analysis Methods,Analysis Method, Karyotype,Analysis Methods, Karyotype,Karyotype Analysis Method,Karyotypings,Method, Karyotype Analysis,Methods, Karyotype Analysis
D008214 Lymphocytes White blood cells formed in the body's lymphoid tissue. The nucleus is round or ovoid with coarse, irregularly clumped chromatin while the cytoplasm is typically pale blue with azurophilic (if any) granules. Most lymphocytes can be classified as either T or B (with subpopulations of each), or NATURAL KILLER CELLS. Lymphoid Cells,Cell, Lymphoid,Cells, Lymphoid,Lymphocyte,Lymphoid Cell
D008297 Male Males
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D002869 Chromosome Aberrations Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS. Autosome Abnormalities,Cytogenetic Aberrations,Abnormalities, Autosome,Abnormalities, Chromosomal,Abnormalities, Chromosome,Chromosomal Aberrations,Chromosome Abnormalities,Cytogenetic Abnormalities,Aberration, Chromosomal,Aberration, Chromosome,Aberration, Cytogenetic,Aberrations, Chromosomal,Aberrations, Chromosome,Aberrations, Cytogenetic,Abnormalities, Cytogenetic,Abnormality, Autosome,Abnormality, Chromosomal,Abnormality, Chromosome,Abnormality, Cytogenetic,Autosome Abnormality,Chromosomal Aberration,Chromosomal Abnormalities,Chromosomal Abnormality,Chromosome Aberration,Chromosome Abnormality,Cytogenetic Aberration,Cytogenetic Abnormality
D002901 Chromosomes, Human, 13-15 The medium-sized, acrocentric human chromosomes, called group D in the human chromosome classification. This group consists of chromosome pairs 13, 14, and 15. Chromosomes D,Group D Chromosomes,Chromosome, Group D,Chromosomes, Group D,Group D Chromosome
D002906 Chromosomes, Human, 6-12 and X The medium-sized, submetacentric human chromosomes, called group C in the human chromosome classification. This group consists of chromosome pairs 6, 7, 8, 9, 10, 11, and 12 and the X chromosome. Chromosomes C,Group C Chromosomes,Chromosomes, Human, 6-12,Chromosome, Group C,Chromosomes, Group C,Group C Chromosome
D005260 Female Females
D005347 Fibroblasts Connective tissue cells which secrete an extracellular matrix rich in collagen and other macromolecules. Fibroblast

Related Publications

T W Hustinx, and B G Ter Haar, and J M Scheres, and F J Rutten
Trisomy for the short arm of chromosome No. 10.
October 1977, Journal de genetique humaine,
T W Hustinx, and B G Ter Haar, and J M Scheres, and F J Rutten
Trisomy of the short arm of chromosome 10.
December 1975, Journal of medical genetics,
T W Hustinx, and B G Ter Haar, and J M Scheres, and F J Rutten
Deletion of the short arm of chromosome No. 10.
September 1977, Acta paediatrica Scandinavica,
T W Hustinx, and B G Ter Haar, and J M Scheres, and F J Rutten
Deletion of the short arm of chromosome No. 10.
March 1975, Journal of medical genetics,
T W Hustinx, and B G Ter Haar, and J M Scheres, and F J Rutten
A new case of trisomy for the short arm of No. 9 chromosome.
September 1973, Journal of medical genetics,
T W Hustinx, and B G Ter Haar, and J M Scheres, and F J Rutten
Trisomy for short arm of chromosome 20.
January 1974, Humangenetik,
T W Hustinx, and B G Ter Haar, and J M Scheres, and F J Rutten
A case of trisomy for the short arm of chromosome no. 9(+9(p)).
September 1976, Human genetics,
T W Hustinx, and B G Ter Haar, and J M Scheres, and F J Rutten
Partial trisomy for short arm of chromosome 5.
August 1993, Acta paediatrica Japonica : Overseas edition,
T W Hustinx, and B G Ter Haar, and J M Scheres, and F J Rutten
Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.
January 1971, Humangenetik,
T W Hustinx, and B G Ter Haar, and J M Scheres, and F J Rutten
[Trisomy of the short arm of chromosome 9].
April 1989, Pediatria polska,
Copied contents to your clipboard!