Palmer C, Conneally P, Yu P
Hum Genet. 1981; 57(4):423-7.
PMID: 7286984
DOI: 10.1007/BF00281697.
Fogle T, McKenzie W
Hum Genet. 1980; 55(3):345-52.
PMID: 7203469
DOI: 10.1007/BF00290216.
Ibraimov A, Mirrakhimov M
Hum Genet. 1982; 62(3):252-7.
PMID: 7169217
DOI: 10.1007/BF00333531.
Meulenbroek G, Geraedts J
Hum Genet. 1982; 62(2):129-33.
PMID: 7160845
DOI: 10.1007/BF00282300.
Fogle T, Namboodiri K, Elston R, McKenzie W, HAMES C
Hum Genet. 1980; 55(3):353-6.
PMID: 6937430
DOI: 10.1007/BF00290217.
Pericentric inversions. Problems and significance for clinical genetics.
Kaiser P
Hum Genet. 1984; 68(1):1-47.
PMID: 6389316
DOI: 10.1007/BF00293869.
Human chromosomal polymorphism. I. Chromosomal Q polymorphism in Mongoloid populations of Central Asia.
Ibraimov A, Mirrakhimov M, Nazarenko S, Axenrod E, Akbanova G
Hum Genet. 1982; 60(1):1-7.
PMID: 6210616
DOI: 10.1007/BF00281253.
Major histocompatibility complex-restricted H-Y-specific antibodies and cytotoxic T lymphocytes may recognize different self determinants.
Goulmy E, van Leeuwen A, Blokland E, van Rood J, Biddison W
J Exp Med. 1982; 155(5):1567-72.
PMID: 6175722
PMC: 2186669.
DOI: 10.1084/jem.155.5.1567.
Human chromosomal heteromorphisms in American blacks. III. Evidence for racial differences in RFA color and QFQ intensity heteromorphisms.
Verma R, Dosik H
Hum Genet. 1981; 56(3):329-37.
PMID: 6165670
DOI: 10.1007/BF00274688.
Human chromosome variation: the discriminatory power of Q-band heteromorphism (variant) analysis in distinguishing between individuals, with specific application to cases of questionable paternity.
Olson S, Magenis R, Lovrien E
Am J Hum Genet. 1986; 38(2):235-52.
PMID: 3946425
PMC: 1684761.
Human chromosomal polymorphism. VIII. Chromosomal Q polymorphism in the Yakut of Eastern Siberia.
Ibraimov A, Mirrakhimov M, Axenrod E
Hum Genet. 1986; 73(2):147-50.
PMID: 3721501
DOI: 10.1007/BF00291605.
Loop formation and synaptic adjustment in a human male heterozygous for two pericentric inversions.
Guichaoua M, Delafontaine D, Taurelle R, Taillemite J, Morazzani M, Luciani J
Chromosoma. 1986; 93(4):313-20.
PMID: 3698745
DOI: 10.1007/BF00327589.
Human chromosomal polymorphism. IX. Further data on the possible selective value of chromosomal Q-heterochromatin material.
Ibraimov A, Mirrakhimov M, Axenrod E, Kurmanova G
Hum Genet. 1986; 73(2):151-6.
PMID: 2941357
DOI: 10.1007/BF00291606.
Inheritance of chromosome heteromorphisms analyzed by high-resolution bivariate flow karyotyping.
Trask B, van den Engh G, Gray J
Am J Hum Genet. 1989; 45(5):753-60.
PMID: 2816941
PMC: 1683447.
Chromosome heteromorphism quantified by high-resolution bivariate flow karyotyping.
Trask B, van den Engh G, Mayall B, Gray J
Am J Hum Genet. 1989; 45(5):739-52.
PMID: 2479266
PMC: 1683437.
Frequency of chromosomal fluorescence polymorphism in normal persons and in clinical patients with diagnosed chromosome aberrations.
Schwinger E, Wehner H
Hum Genet. 1976; 32(2):115-9.
PMID: 1270069
DOI: 10.1007/BF00291493.
Minor chromosome variations and selected heteromorphisms in 200 unclassifiable mentally retarded patients and 200 normal controls.
Tharapel A, Summitt R
Hum Genet. 1978; 41(2):121-30.
PMID: 640651
DOI: 10.1007/BF00273094.
Variant chromosome 3 (inv3) in normal newborns and their parents, and in children with mental retardation.
Mikelsaar A, Ilus T, Kivi S
Hum Genet. 1978; 41(1):109-13.
PMID: 631855
DOI: 10.1007/BF00278877.
Twins and Q-banded chromosome polymorphisms.
McCracken A, Daly P, Zolnick M, Clark A
Hum Genet. 1978; 45(3):253-8.
PMID: 570167
DOI: 10.1007/BF00278724.
The quantitative analysis of polymorphism on human chromosomes 1, 9, 16, and Y. II. Comparison of the C segments in male and female individuals (group characteristics).
Podugolnikova O, Sushanlo H, Parfenova I, PROKOFIEVA-BELGOVSKAJA A
Hum Genet. 1979; 49(3):251-60.
PMID: 478534
DOI: 10.1007/BF00569344.