BIOMAT Database Logo BIOMAT Database Logo

Partial trisomy of chromosome 1 resulting from a complex maternal rearrangement of chromosomes 1, 5, and 6. 1979

T W Hustinx, and F A Nabben, and J M Scheres

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
D008297 Male Males
D002900 Chromosomes, Human, 1-3 The large, metacentric human chromosomes, called group A in the human chromosome classification. This group consists of chromosome pairs 1, 2, and 3. Chromosomes A,Group A Chromosomes,Chromosome, Group A,Chromosomes, Group A,Group A Chromosome
D002905 Chromosomes, Human, 4-5 The large, submetacentric human chromosomes, called group B in the human chromosome classification. This group consists of chromosome pairs 4 and 5. Chromosomes B,Group B Chromosomes,Chromosome, Group B,Chromosomes, Group B,Group B 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
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000015 Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. Multiple Abnormalities
D014178 Translocation, Genetic A type of chromosome aberration characterized by CHROMOSOME BREAKAGE and transfer of the broken-off portion to another location, often to a different chromosome. Chromosomal Translocation,Translocation, Chromosomal,Chromosomal Translocations,Genetic Translocation,Genetic Translocations,Translocations, Chromosomal,Translocations, Genetic
D014314 Trisomy The possession of a third chromosome of any one type in an otherwise diploid cell. Partial Trisomy,Chromosomal Triplication,Chromosomal Triplications,Partial Trisomies,Trisomies,Trisomies, Partial,Trisomy, Partial

Related Publications

T W Hustinx, and F A Nabben, and J M Scheres
Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.
April 1974, Humangenetik,
T W Hustinx, and F A Nabben, and J M Scheres
Partial trisomy 4 resulting from a complex maternal rearrangement of chromosomes 2, 4, and 18 with interstitial translocation.
September 1979, Human genetics,
T W Hustinx, and F A Nabben, and J M Scheres
Partial trisomy 22 in a liveborn resulting from a rearrangement between chromosomes 6 and 22.
September 2000, Journal of medical genetics,
T W Hustinx, and F A Nabben, and J M Scheres
Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation.
February 1978, Journal of medical genetics,
T W Hustinx, and F A Nabben, and J M Scheres
Partial trisomy 11,46,XX,-3,-20, + der3, + der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20.
February 1976, Human genetics,
T W Hustinx, and F A Nabben, and J M Scheres
A complex chromosome rearrangement resulting in trisomy 15q22 to qter.
June 1982, Journal of medical genetics,
T W Hustinx, and F A Nabben, and J M Scheres
Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.
December 1997, American journal of medical genetics,
T W Hustinx, and F A Nabben, and J M Scheres
Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10.
December 2011, Molecular cytogenetics,
T W Hustinx, and F A Nabben, and J M Scheres
Partial trisomy 16q resulting from maternal translocation.
June 1979, Human genetics,
T W Hustinx, and F A Nabben, and J M Scheres
Partial trisomy 6p and partial trisomy 22 resulting from 3:1 meiotic disjunction of maternal (6p;22q) translocation.
April 1986, Journal of medical genetics,
Copied contents to your clipboard!