Works matching IS 00099163 AND DT 1975 AND VI 8 AND IP 5
Results: 34
Free Topic Meeting: Meiotic Chromosomes in Man and other Mammals.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 394, doi. 10.1111/j.1399-0004.1975.tb01535.x
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Lateral asymmetry of gonadal growth and differentiation.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 392, doi. 10.1111/j.1399-0004.1975.tb01531.x
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Gene activity in early mammalian development.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 391, doi. 10.1111/j.1399-0004.1975.tb01526.x
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The development of haploid and diploid parthenogenetic mouse embryos.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 387, doi. 10.1111/j.1399-0004.1975.tb01520.x
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Differentiation of male germinal cells in vitro.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 395, doi. 10.1111/j.1399-0004.1975.tb01536.x
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Studies on mouse-bank vole interspecific chimaeric embryos.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 388, doi. 10.1111/j.1399-0004.1975.tb01521.x
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Satellite association: Giemsa banding studies in parents of Down's syndrome patients.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 319, doi. 10.1111/j.1399-0004.1975.tb01509.x
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Characterization of foetal cells in maternal blood.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 391, doi. 10.1111/j.1399-0004.1975.tb01527.x
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G-banding of meiotic chromosomes in the male: pachytene analysis of the 22 autosomes.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 395, doi. 10.1111/j.1399-0004.1975.tb01537.x
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Trisomy 9q - a new syndrome.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 392, doi. 10.1111/j.1399-0004.1975.tb01530.x
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Gene activity in early mammalian development.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 390, doi. 10.1111/j.1399-0004.1975.tb01525.x
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Developmental studies on molested mice: chimaeras and tetraploids.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 388, doi. 10.1111/j.1399-0004.1975.tb01522.x
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Molecular genetics of GM.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 303, doi. 10.1111/j.1399-0004.1975.tb01507.x
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International Registry of Abnormal Karyotypes.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 383, doi. 10.1111/j.1399-0004.1975.tb01518.x
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Influence of the myopia gene on brain development.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 314, doi. 10.1111/j.1399-0004.1975.tb01508.x
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Partial deletions and trisomies of chromosome 13. Mapping in relation to the chromosome 13 banding.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 394, doi. 10.1111/j.1399-0004.1975.tb01534.x
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Hyperpipecolic acidemia associated with hepatomegaly, mental retardation, optic nerve dysplasia and progressive neurological disease.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 376, doi. 10.1111/j.1399-0004.1975.tb01517.x
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Genetic regulatory systems for mammalian sexual development.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 387, doi. 10.1111/j.1399-0004.1975.tb01519.x
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Variable expression of Marfan syndrome in monozygotic twins.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 358, doi. 10.1111/j.1399-0004.1975.tb01514.x
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Journal of Immunogenetics.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 398, doi. 10.1111/j.1399-0004.1975.tb01540.x
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- Article
Comparison of the chromosomal maps of chimpanzee and man.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 392, doi. 10.1111/j.1399-0004.1975.tb01529.x
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Position effect variegation/X inactivation in the mouse.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 389, doi. 10.1111/j.1399-0004.1975.tb01524.x
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Two cases of the chromatin positive variety of ovarian dysgenesis (XO/XX mosaicism) associated with hGH deficiency and marginal impairment of other hypothalamic-pituitary functions.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 324, doi. 10.1111/j.1399-0004.1975.tb01510.x
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Origin of a small metacentric chromosome: Familial and cytogenetic evidence.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 364, doi. 10.1111/j.1399-0004.1975.tb01515.x
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Announcements.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 397, doi. 10.1111/j.1399-0004.1975.tb01539.x
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Developmental aspects of amino acid transport: switching-on and switching-off mechanism.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 393, doi. 10.1111/j.1399-0004.1975.tb01533.x
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The Nathalie syndrome. A new hereditary syndrome.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 330, doi. 10.1111/j.1399-0004.1975.tb01511.x
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Ring chromosome 6 in a malformed boy.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 370, doi. 10.1111/j.1399-0004.1975.tb01516.x
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Fetal loss and familial chromosome I translocations.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 341, doi. 10.1111/j.1399-0004.1975.tb01512.x
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Y-chromatin frequency in the blood of pregnant women during pregnancy.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 392, doi. 10.1111/j.1399-0004.1975.tb01528.x
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Meiosis in human male sterility: report of 27 cases with a common anomaly.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 396, doi. 10.1111/j.1399-0004.1975.tb01538.x
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The 9p- deletion syndrome. Report of a patient with a 46, XX, 9p- constitution due to a paternal t(9p-; 15q+) translocation.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 349, doi. 10.1111/j.1399-0004.1975.tb01513.x
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Morphogenesis in trisomic mouse embryos.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 389, doi. 10.1111/j.1399-0004.1975.tb01523.x
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Embryonic hemoglobins.
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- Clinical Genetics, 1975, v. 8, n. 5, p. 393, doi. 10.1111/j.1399-0004.1975.tb01532.x
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