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Human Genetics|January 1, 1983
Fragile chromosome 16(q22) cause a balanced translocation at the same pointJ M García-Sagredo, C San Román, M E Gallego Gómez, et al.Human Genetics|January 1, 1983
Increased satellite association induced by 5' bromodeoxyuridine treatment of phytohemaglutinin-stimulated blood lymphocytesJ Musilová, K Michalová, H HoffmanováHuman Genetics|January 1, 1983
Silver staining of nucleolus organizer regions during human spermatogenesisM Schmid, H Müller, S Stasch, et al.Human Genetics|January 1, 1983
Red cell glyoxalase I polymorphism in Basque and Castilian populationsM Martínez de Pancorbo, M Isusquiza, A I Aguirre, et al.Human Genetics|January 1, 1983
Complete or partial trisomy for the long arm of chromosome 1 in patients with various hematologic malignanciesS E Mamaeva, N N Mamaev, N M Jartseva, et al.Human Genetics|January 1, 1984
Transmission of the marker X syndrome trait by unaffected males: conclusions from studies of large familiesU Froster-Iskenius, A Schulze, E SchwingerHuman Genetics|January 1, 1983
A search for linkage in families with fragile sitesJ C Mulley, C Nicholls, G R SutherlandHuman Genetics|June 29, 1976
Prenatal diagnosis of congenital anomalies in an intrauterine growth retarded fetusM S Golbus, B D Hall, R K CreasyHuman Genetics|January 1, 1984
Isochromosome 6p, a unique chromosomal abnormality in retinoblastoma: verification by standard staining techniques, new densitometric methods, and somatic cell hybridizationJ Squire, R A Phillips, S Boyce, et al.Human Genetics|April 15, 1977
DIPI and DAPI: fluorescence banding with only negliglible fadingW Schnedl, A V Mikelsaar, M Breitenbach, et al.Pageof 959