BIOMAT Database Logo BIOMAT Database Logo

Trisomy 20q due to maternal t(16;20) translocation. First case. 1979

I H Pawlowitzki, and H Gröbe, and W Holzgreve

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D002871 Chromosome Banding Staining of bands, or chromosome segments, allowing the precise identification of individual chromosomes or parts of chromosomes. Applications include the determination of chromosome rearrangements in malformation syndromes and cancer, the chemistry of chromosome segments, chromosome changes during evolution, and, in conjunction with cell hybridization studies, chromosome mapping. Banding, Chromosome,Bandings, Chromosome,Chromosome Bandings
D002902 Chromosomes, Human, 16-18 The short, submetacentric human chromosomes, called group E in the human chromosome classification. This group consists of chromosome pairs 16, 17, and 18. Chromosomes E,Group E Chromosomes,Chromosome, Group E,Chromosomes, Group E,E Chromosomes, Group,Group E Chromosome
D002903 Chromosomes, Human, 19-20 The short, metacentric human chromosomes, called group F in the human chromosome classification. This group consists of chromosome pairs 19 and 20. Chromosomes F,Group F Chromosomes,Chromosome, Group F,Chromosomes, Group F,Group F Chromosome
D005260 Female Females
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

I H Pawlowitzki, and H Gröbe, and W Holzgreve
9p trisomy: a new case due to maternal t(9;18) translocation.
January 1977, Acta geneticae medicae et gemellologiae,
I H Pawlowitzki, and H Gröbe, and W Holzgreve
Partial trisomy 20q due to paternal t(8;20) translocation. Case report and review of the literature.
May 1988, Clinical genetics,
I H Pawlowitzki, and H Gröbe, and W Holzgreve
[Trisomy 20p due to balanced maternal translocation t(3;20)].
January 1979, Pathologica,
I H Pawlowitzki, and H Gröbe, and W Holzgreve
[Partial trisomy 13 due to maternal translocation t(2;13)].
September 1977, Annales de genetique,
I H Pawlowitzki, and H Gröbe, and W Holzgreve
Partial trisomy 6p due to maternal t(1;6) translocation.
June 1996, Clinical genetics,
I H Pawlowitzki, and H Gröbe, and W Holzgreve
Interchange trisomy 9 due to maternal t(6;9) translocation.
October 1994, Acta paediatrica Japonica : Overseas edition,
I H Pawlowitzki, and H Gröbe, and W Holzgreve
[lq32qter trisomy due to maternal translocation t(1;6) (q32; q26)].
January 1979, Pathologica,
I H Pawlowitzki, and H Gröbe, and W Holzgreve
Partial trisomy 18 due to a maternal translocation t(9;18).
January 1984, Human genetics,
I H Pawlowitzki, and H Gröbe, and W Holzgreve
Partial trisomy 13 due to maternal translocation t(7;13)(p22q14).
January 1982, Annales de genetique,
I H Pawlowitzki, and H Gröbe, and W Holzgreve
[Partial trisomy 15q due to maternal translocation t(7;15)(q35;14)].
March 1976, Annales de genetique,
Copied contents to your clipboard!