BIOMAT Database Logo BIOMAT Database Logo

Abnormalities resulting from a familial pericentric inversion of chromosome 18. 1978

M K Kukolich, and B W Althaus, and J W Sears, and C B Mankinen, and R C Lewandowski

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D007446 Chromosome Inversion An aberration in which a chromosomal segment is deleted and reinserted in the same place but turned 180 degrees from its original orientation, so that the gene sequence for the segment is reversed with respect to that of the rest of the chromosome. Inversion, Chromosome,Inversion, Chromosomal,Chromosomal Inversion,Chromosomal Inversions,Chromosome Inversions,Inversions, Chromosomal,Inversions, Chromosome
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
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
D002478 Cells, Cultured Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others. Cultured Cells,Cell, Cultured,Cultured Cell
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
D003878 Dermatoglyphics The study of the patterns of ridges of the skin of the fingers, palms, toes, and soles. Fingerprints,Plantar Prints,Fingerprint,Plantar Print,Print, Plantar,Prints, Plantar
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

Related Publications

M K Kukolich, and B W Althaus, and J W Sears, and C B Mankinen, and R C Lewandowski
Recombinant chromosome 18 resulting from a maternal pericentric inversion.
May 1994, American journal of medical genetics,
M K Kukolich, and B W Althaus, and J W Sears, and C B Mankinen, and R C Lewandowski
Familial 10p trisomy resulting from a maternal pericentric inversion.
February 1994, American journal of medical genetics,
M K Kukolich, and B W Althaus, and J W Sears, and C B Mankinen, and R C Lewandowski
Familial pericentric inversion of chromosome 2.
June 1981, Journal de genetique humaine,
M K Kukolich, and B W Althaus, and J W Sears, and C B Mankinen, and R C Lewandowski
Familial pericentric inversion of chromosome 8.
January 1981, American journal of medical genetics,
M K Kukolich, and B W Althaus, and J W Sears, and C B Mankinen, and R C Lewandowski
Familial pericentric inversion of chromosome 12.
April 1986, Human genetics,
M K Kukolich, and B W Althaus, and J W Sears, and C B Mankinen, and R C Lewandowski
Familial pericentric inversion of chromosome 13 resulting in duplication 13q22 to qter.
June 1982, Journal of medical genetics,
M K Kukolich, and B W Althaus, and J W Sears, and C B Mankinen, and R C Lewandowski
[Pericentric inversion of chromosome Y. Familial study].
January 1982, Pathologica,
M K Kukolich, and B W Althaus, and J W Sears, and C B Mankinen, and R C Lewandowski
Familial pericentric inversion of the Y chromosome.
January 1984, Annales de genetique,
M K Kukolich, and B W Althaus, and J W Sears, and C B Mankinen, and R C Lewandowski
[Chromosome 18 partial duplication-deficiency by recombination aneusomia in familial pericentric inversion].
April 1980, Annales de pediatrie,
M K Kukolich, and B W Althaus, and J W Sears, and C B Mankinen, and R C Lewandowski
Partial trisomy 20p resulting from a recombination of a familial pericentric inversion.
December 1986, Human genetics,
Copied contents to your clipboard!