Partial deletion of short arm of chromosome 18. 1984

P Kiss, and M Osztovics, and G Kosztolányi, and A Papp

Three cases of partial deletion of the short arm of chromosome 18 (pll-pter) are presented. The cytogenetic and clinical features of the patients observed are compared to cases found in the literature. 18p-aberration produces a fairly unique phenotypic alteration, but on the sole basis of the clinical manifestation, without cytogenetic analysis, correct diagnosis cannot be established.

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. 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
D011596 Psychomotor Disorders Abnormalities of motor function that are associated with organic and non-organic cognitive disorders. Psychomotor Impairment,Developmental Psychomotor Disorders,Psychomotor Disorders, Developmental,Developmental Psychomotor Disorder,Impairment, Psychomotor,Impairments, Psychomotor,Psychomotor Disorder, Developmental,Psychomotor Impairments
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
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
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
D003582 Cytogenetics A subdiscipline of genetics which deals with the cytological and molecular analysis of the CHROMOSOMES, and location of the GENES on chromosomes, and the movements of chromosomes during the CELL CYCLE. Cytogenetic
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

P Kiss, and M Osztovics, and G Kosztolányi, and A Papp
November 1967, The Tohoku journal of experimental medicine,
P Kiss, and M Osztovics, and G Kosztolányi, and A Papp
June 1970, Annales de genetique,
P Kiss, and M Osztovics, and G Kosztolányi, and A Papp
January 1966, Annales de genetique,
P Kiss, and M Osztovics, and G Kosztolányi, and A Papp
January 1964, Cytogenetics,
P Kiss, and M Osztovics, and G Kosztolányi, and A Papp
April 1968, American journal of diseases of children (1960),
P Kiss, and M Osztovics, and G Kosztolányi, and A Papp
January 1969, Humangenetik,
P Kiss, and M Osztovics, and G Kosztolányi, and A Papp
September 1964, American journal of human genetics,
P Kiss, and M Osztovics, and G Kosztolányi, and A Papp
December 1975, Annales de genetique,
P Kiss, and M Osztovics, and G Kosztolányi, and A Papp
May 1971, The Journal of pediatrics,
P Kiss, and M Osztovics, and G Kosztolányi, and A Papp
June 1986, Clinical genetics,
Copied contents to your clipboard!