Risk for recombinants in pericentric inversions of the (p11→q21) region of chromosome 18 V. VigiPaola MaraschioM. Fraccaro Original Articles Pages: 1 - 5
Parental origin of the extra chromosome in Down's syndrome R. E. MagenisK. M. OvertonE. Lovrien Original Investigations Pages: 7 - 16
Partial trisomy 8q in half-sisters with distinct dysmorphic patterns not similar to the trisomy 8 mosaicism syndrome A. Schinzel Original Investigations Pages: 17 - 26
Sister chromatid exchanges in balanced translocation carriers and in patients with unbalanced karyotypes C. StollD. S. BorgaonkarP. Bigel Original Investigations Pages: 27 - 32
Karyotyping of bone-marrow cells in hematologic diseases H. G. MorseJ. R. HumbertA. Robinson Original Investigations Pages: 33 - 39
HLA-A, B, C gene and haplotype frequencies in Vienna Wolfgang R. Mayr Original Investigations Pages: 41 - 48
The red-cell glutamic-pyruvate transaminase, carbonic anhydrase I and II and esterase D polymorphisms in the Ambo populations of South West Africa, with evidence for the existence of an EsD 0 allele Marion P. MarksTrefor JenkinsG. T. Nurse Original Investigations Pages: 49 - 54
Human DNA replication: Fiber autoradiographic analysis of diploid cells from normal adults and from Fanconi's anemia and ataxia telangiectasia Roger Hand Original Investigations Pages: 55 - 64
Localization of chromatid breaks in Fanconi's anemia, using three consecutive stains B. DutrillauxJ. CouturierG. Schaison Original Investigations Pages: 65 - 71
Frequency of Ag-stained nucleolus organizer regions in the acrocentric chromosomes of man A. V. MikelsaarM. SchmidW. Schnedl Short Communications Pages: 73 - 77
Combined silver staining of the nucleolus organizing regions and Giemsa banding in human chromosomes H. ZanklS. Bernhardt Short Communications Pages: 79 - 80
Recurrent abortion associated with a balanced 22;22 translocation, or isochromosome 22q in a monozygous twin B. V. LewisM. A. C. Ridler Short Communications Pages: 81 - 85
Ring chromosome 4 and wolf syndrome Amalia Pérez-CastilloJ. A. Abrisqueta Clinical Case Reports Pages: 87 - 91
Short-arm deletion of an X chromosome (45,XO/46,XX p-) P. KaiserK. Gerhard-RatschowE. Daume Clinical Case Reports Pages: 93 - 96
Familial t(X;2) (p223;q323) with partial trisomy 2q and male and female balanced carriers Catherine TurleauFrançoise Chavin-ColinP. Beauvais Clinical Case Reports Pages: 97 - 104
Partial trisomy 14q due to familial t(14q-, 11q+) translocation J. P. FrynsM. Van EygenH. Van Den Berghe Clinical Case Reports Pages: 105 - 110
47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)mat E. KesselR. A. Pfeiffer Clinical Case Reports Pages: 111 - 116
Pure gonadal dysgenesis (Type XX) H. R. S. de NazarethL. M. S. FarahF. J. P. B. Vieira Clinical Case Reports Pages: 117 - 120
Dispermic origin of a 69,XXY triploid Nora L. BlackwellJean W. KeelingRichard H. Lindenbaum Clinical Case Reports Pages: 121 - 124
