Segregation of marker loci in families with an inherited paracentric insertion of chromosome 9

Authors :: Allderdice, P W
Kaita, H
Lewis, M
McAlpine, P J
Wong, P
Anderson, J
Giblett, E R
Publication Year :: 1986
Abstract: Cytogenetic, enzyme dosage, serological, and electrophoretic analyses of blood samples from members of three Newfoundland kindreds in which one specific paracentric insertion chromosome inv ins(9)(q22.1q34.3q34.1) is segregating provide data indicating that ABO lies in 9q22.1-q34.3, AK1 in 9q34.1-q34.3, and ORM in 9q34.3-qter.

Subjects :: Chromosome Aberrations
Genetic Markers
congenital, hereditary, and neonatal diseases and abnormalities
Adenylate Kinase
Phosphotransferases
Chromosome Mapping
Chromosome Disorders
Orosomucoid
ABO Blood-Group System
Pedigree
hemic and lymphatic diseases
Humans
Crossing Over, Genetic
Chromosome Deletion
Chromosomes, Human, Pair 9
Research Article

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