BIOMAT Database Logo BIOMAT Database Logo

Partial E-18 long-arm deletion. 1968

W E Nance, and S H Higdon, and B Chown, and E Engel

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
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
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D025063 Chromosome Disorders Clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material (either a whole chromosome or a chromosome segment). (from Thompson et al., Genetics in Medicine, 5th ed, p429) Autosomal Chromosome Disorders,Chromosome Abnormality Disorders,Chromosomal Disorders,Autosomal Chromosome Disorder,Chromosomal Disorder,Chromosome Abnormality Disorder,Chromosome Disorder,Chromosome Disorder, Autosomal,Chromosome Disorders, Autosomal,Disorder, Chromosomal,Disorder, Chromosome,Disorder, Chromosome Abnormality,Disorders, Chromosomal,Disorders, Chromosome

Related Publications

W E Nance, and S H Higdon, and B Chown, and E Engel
Partial deletion of the long arm of chromosome E-18.
November 1970, Pediatrics,
W E Nance, and S H Higdon, and B Chown, and E Engel
Partial deletion of the long arm of chromosome 18.
January 1969, Humangenetik,
W E Nance, and S H Higdon, and B Chown, and E Engel
Partial deletion of short arm of chromosome 18.
January 1984, Acta paediatrica Hungarica,
W E Nance, and S H Higdon, and B Chown, and E Engel
[18 Q-syndrome. A new case of partial deletion of the long arm of chromosome 18].
May 1974, Annales medico-psychologiques,
W E Nance, and S H Higdon, and B Chown, and E Engel
[Partial deletion of the long arm of chromosome 18. Individualization of a new morbid state].
January 1966, Annales de genetique,
W E Nance, and S H Higdon, and B Chown, and E Engel
[Chromosome 18 long-arm deletion. Report of 1 case].
November 1980, Anales espanoles de pediatria,
W E Nance, and S H Higdon, and B Chown, and E Engel
Partial deletion of long arms of chromosome 18.
July 1968, Pediatrics,
W E Nance, and S H Higdon, and B Chown, and E Engel
[The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
June 1967, Annales de genetique,
W E Nance, and S H Higdon, and B Chown, and E Engel
Deletion on long arm of a chromosome 18 (46, XX, 18 q-).
November 1967, Humangenetik,
W E Nance, and S H Higdon, and B Chown, and E Engel
[Chromosome X with partial long arm deletion. Three cases].
January 1992, Journal de gynecologie, obstetrique et biologie de la reproduction,
Copied contents to your clipboard!