Human chromosomal polymorphism. I. Chromosomal Q polymorphism in Mongoloid populations of central Asia A. I. IbraimovM. M. MirrakhimovG. A. Akbanova Original Investigations Pages: 1 - 7
Human chromosomal polymorphism. II. Chromsomal C polymorphism in Mongoloid populations of central Asia A. I. IbraimovM. M. MirrakhimovE. I. Axenrod Original Investigations Pages: 8 - 9
Assigning the polymorphic human insulin gene to the short arm of chromosome 11 by chromosome sorting Roger V. LeboYuet Wai KanHoward M. Goodman Original Investigations Pages: 10 - 15
Distinction électrophorétique entre les deux sous-espèces d'Orang-outan G. LucotteD. G. Smith Original Investigations Pages: 16 - 18
Variation in the sensitivity of human lymphocttes to DNA-damaging agents measured by sister chromatid exchange frequency Peter E. Crossen Original Investigations Pages: 19 - 23
Genetic determination of NOR activity in human lymphocytes from twins A. F. ZakharovA. Z. DavudovN. A. Egolina Original Investigations Pages: 24 - 29
Controlled trial of serum isoelectric focusing in the detection of the cystic fibrosis gene David J. H. BrockCaroline HaywardMaurice Super Original Investigations Pages: 30 - 31
Evidence for duplication of the human salivary amylase gene Jan C. PronkRune R. FrantsGerard J. M. Tonino Original Investigations Pages: 32 - 35
A distinct osteochondrodysplasia with hypertrichosis—Individualization of a probable autosomal recessive entity J. M. CantúD. Garcia-CruzZ. Nazará Original Investigations Pages: 36 - 41
Polymorphism of properdin factor B in Japanese. Description of a rare variant and data of association with HLA and C2 K. TokunagaC. ArakiK. Omoto Original Investigations Pages: 42 - 45
Rabl's model of the interphase chromosome arrangement tested in Chinise hamster cells by premature chromosome condensation and laser-UV-microbeam experiments T. CremerC. CremerC. Zorn Original Investigations Pages: 46 - 56
Genetic polymorphism of human plasminogen in the Japanese population: New plasminogen variants and relationship between plasminogen phenotypes and their biological activities Shigeki NakamuraKazue Abe Original Investigations Pages: 57 - 59
Glucose 6-phosphate dehydrogenase variants of Bali Island (Indonesia) K. ChockkalingamP. G. BoardG. Breguet Original Investigations Pages: 60 - 62
Cytogenetic findings in 4952 prenatal diagnoses. An Italian collaborative study G. SimoniM. FraccaroM. G. Tibiletti Original Investigations Pages: 63 - 68
Elevated levels of arylsulfatase C activity in cultured skin fibroblasts of patients with autosomal dominant ichthyosis vulgaris J. Ch. MeyerHanspeter GrundmannHeidi Weiss Short Communications Pages: 69 - 70
HLA typing in a new family with fletcher factor deficiency C. RaffouxP. AlexandreF. Streiff Short Communications Pages: 71 - 73
Moderate Down's syndrome in three siblings having partial trisomy 21q22.2→qter and therefore no SOD-1 excess M. HabedankA. Rodewald Clinical Case Reports Pages: 74 - 77
Maternally transmitted extra ring(21) chromosome in a boy with Down's syndrome Takako MatsubaraYasuo NakagomeTsunehiro Yokochi Clinical Case Reports Pages: 78 - 79
Methods of increasing the visibility of fragile X chromosomes Heinrich ZanklGertrud Eberle Clinical Case Reports Pages: 80 - 81
An XX male with a 46,XX/47,XX,+Y(q12→qter) karyotype Rosa MiróM. Rosa CaballínJ. Egozcue Clinical Case Reports Pages: 82 - 84
Cytogenetic studies in a Y-to-X translocation observed in three members of one family, with evidence of infertility in male carriers Kiyomi YamadaShinichiro NankoKoichiro Isurugi Clinical Case Reports Pages: 85 - 90
Ring chromosome 2: Clinical, chromosomal, and biochemical aspects M. JansenF. A. BeemerJ. L. Van den Brande Clinical Case Reports Pages: 91 - 95
