Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15 R. R. SchreckW. R. BregO. J. Miller Original Investigations 01 January 1977 Pages: 1 - 12
Dermatoglyphic differences between 45,X and other chromosomal abnormalities of Turner syndrome T. ReedA. ReichmannC. G. Palmer Original Investigations 01 January 1977 Pages: 13 - 23
Partial trisomy of the long arm of human chromosome 1 as demonstrated by in situ hybridization with 5S ribosomal RNA Dale M. SteffensenErnest H. Y. ChuRobert P. Kelch Original Investigations 01 January 1977 Pages: 25 - 33
Partial trisomy 12p due to t(12;21)pat translocation B. BiedermanP. BowenD. Schiff Original Investigations 01 January 1977 Pages: 35 - 41
An unexpected high frequency of trisomic fetuses in 229 pregnancies monitored for advanced maternal age E. S. SachsM. G. J. JahodaH. Galjaard Original Investigations 01 January 1977 Pages: 43 - 46
On consanguineous marriages and the genetic load Ranajit ChakrabortyAravinda Chakravarti Original Investigations 01 January 1977 Pages: 47 - 54
N-Band polymorphism of human acrocentric chromosomes and its relevance to satellite association Isamu HayataMitsuo OshimuraAvery A. Sandberg Original Investigations 01 January 1977 Pages: 55 - 61
The localization of rDNA in small, nucleolus-like structures in human diplotene oocyte nuclei Debra J. Wolgemuth-JarashowGeorgiana M. JagielloAnn S. Henderson Original Investigations 01 January 1977 Pages: 63 - 68
Elevated sister chromatid exchange rate in lymphocytes of subjects treated with arsenic Walter BurgdorfKaren KurvinkJaroslav Cervenka Original Investigations 01 January 1977 Pages: 69 - 72
Genetic variants of cytoplasmic malate dehydrogenase (MDH:EC:1.1.1.37) in populations in England and the Indian subcontinent S. S. PapihaD. F. RobertsK. C. Shah Original Investigations 01 January 1977 Pages: 73 - 79
Genetic studies of the Macushi and Wapishana Indians James V. NeelRobert J. TanisSally Bachofer Original Investigations 01 January 1977 Pages: 81 - 107
Bf polymorphism: Another variant (S0.8) G. HauptmannE. WertheimerS. Mayer Short Communications 01 January 1977 Pages: 109 - 111
“de novo” trisomy 1q32→1qter and monosomy 3p25→3pter Emilio YunisHernán EgelMyriam Leibovici Clinical Case Reports 01 January 1977 Pages: 113 - 116
A girl with partial long-arm deletion of chromosome 11 and familial pericentric inversion of chromosome 9 Bernhard ZabelSusanne HansenHelga Gröting-Imhof Clinical Case Reports 01 January 1977 Pages: 117 - 122
Translocation D/D involving two homologous chromosomes of the pair 15 Jan ŽižkaPetr BalíĉekAlena Finková Clinical Case Reports 01 January 1977 Pages: 123 - 125
The consequences of the Philadelphia chromosome rearrangement in chronic myeloid leukemia Frederick HechtBarbara Kaiser McCaw Letters to the Editors 01 January 1977 Pages: 127 - 128