Ohga S, Nakao F, Narazaki O, Fusazaki N, Aoki T, Kamesaki K
Arch Dis Child. 1997; 77(3):252-4.
PMID: 9370908
PMC: 1717297.
DOI: 10.1136/adc.77.3.252.
Fischer P, Golob E, Friedrich F, KUNZE-MUHL E, DOLESCHEL W, AICHMAIR H
J Med Genet. 1970; 7(1):91-8.
PMID: 5480972
PMC: 1468926.
DOI: 10.1136/jmg.7.1.91.
DUMARS K, Carnahan L, Barrett R
J Med Genet. 1970; 7(1):86-90.
PMID: 5480971
PMC: 1468912.
DOI: 10.1136/jmg.7.1.86.
Stewart J, Go S, Ellis E, Robinson A
J Med Genet. 1970; 7(1):11-9.
PMID: 5480960
PMC: 1468899.
DOI: 10.1136/jmg.7.1.11.
Finley S, Cooper M, Finley W, UCHIDA I, NOTO T, Roddam R
J Med Genet. 1969; 6(4):388-93.
PMID: 5391901
PMC: 1468779.
DOI: 10.1136/jmg.6.4.388.
Gene deletion and duplication effects on phenotype and gamma globulin levels.
Rudd N, Lamarche P
J Med Genet. 1971; 8(1):97-106.
PMID: 5098075
PMC: 1468971.
DOI: 10.1136/jmg.8.1.97.
The syndrome associated with the partial deletion of the long arms of chromosome 18 (18q-).
Parker C, Mavalwala J, Koch R, Hatashita A, Derencsenyi A
Calif Med. 1972; 117(4):65-71.
PMID: 5075725
PMC: 1518736.
Population cytogenetics, assignment of gene loci in autosomes, karyotype-phenotype correlations. A progress report on human cytogenetics.
Passarge E
Humangenetik. 1970; 9(1):1-15.
PMID: 4922977
DOI: 10.1007/BF00696007.
A special role of the group 17,18 chromosomes in reticuloendothelial neoplasia.
Spiers A, BAIKIE A
Br J Cancer. 1970; 24(1):77-91.
PMID: 4913770
PMC: 2008513.
DOI: 10.1038/bjc.1970.11.
[Ring chromosome 18. 18p-/18q- -deletion-syndrome].
Kunze J, Stephan E, Tolksdorf M
Humangenetik. 1972; 15(4):289-318.
PMID: 4565746
DOI: 10.1007/BF00281730.
Partial monosomies 18. Review of cytogenetical and phenotypical variants.
Lurie I, Lazjuk G
Humangenetik. 1972; 15(3):203-22.
PMID: 4563067
DOI: 10.1007/BF00702354.
Deletion of the long arms of chromosome 18 (46,XX,18q-) associated with absence of IgA and hypothyroidism in an adult.
FAED M, Whyte R, Paterson C, McCathie M, Robertson J
J Med Genet. 1972; 9(1):102-5.
PMID: 4112566
PMC: 1469190.
DOI: 10.1136/jmg.9.1.102.
Four families with immunodeficiency and chromosome abnormalities.
Candy D, Hayward A, Hughes D, Layward L, Soothill J
Arch Dis Child. 1979; 54(7):518-23.
PMID: 314782
PMC: 1545485.
DOI: 10.1136/adc.54.7.518.
