Biomedical subjects
E B Hook
Publications and source records attributed to E B Hook.
Early in vitro division of PHA stimulated cord blood lymphocytes: implications for study of chromosome breakage.
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Apparent "in situ" clone of cytogenetically marked ataxia-telangiectasia lymphocytes.
Six adjacent metaphases, each with the same cytogenetic aberration of a group D chromosome, most probably a No. 14, were observed in a field of a slide from a 96-hour culture of lymphocytes from an individual with ataxia-telangiectasia (AT). None of the 304 other metaphases examined from this or other simultaneous cultures of this individual showed such an aberration. It seems most likely that an "in situ" marked clone has been observed and this supports interpretation of consistent cytogenetic abnormalities in those with AT as having clonal origin. The method of slide preparation employed which involves placing, rather than dropping, the cell suspension on the slide may facilitate detection of "in situ" clones.
Letter: Comment on comparison of settings for study of the prevalence of XYY genotype.
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Parathenar palmar pattern: a dermatoglyphic sign of possible clinical significance.
The frequency of a 'double proximal axial triradius' (DPAT), which results in a palmar parathenar pattern, has been reported to be increased in those with ventricular septal defect (BSD). We scored the presence of this pattern in 313 patients with congenital heart defects (including 86 with isolated VSD), 176 with cystic fibrosis (CF) or relatives of those with CF, and 333 with no known clinical disease who were unrelated to individuals with CF. The frequencies in these three groups were 1.6, 2.3, and 0.6%, respectively. None of those with isolated VSD defect had a DPAT. All five individuals in the heart defect group with a DPAT had pulmonic stenosis. Of the total of eleven individuals in our series with DPAT patterns, eight were affected only on the right hand. The frequency of DPAT in individuals with no known disease in this series was 4/406=1.0%, more than double the frequency in a control series, published previously by DAVID, 5/1,129=0.4%. If the 73 relatives of those with CF are excluded from our own 'control' group, the frequency of DPAT in this group is then 0.6%, closer to the results in DAVID's control series.
Letter: Question regarding pooled data.
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Negative outcome of a blind assessment of the association between spray adhesive exposure and human chromosome breakage.
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Letter: Vitamin E: teratogen or anti-teratogen?
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Letter: Report of Down's syndrome during a period of suspected increase in trisomy 18.
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The distalmost palmar axial triradius in children with selected types of isolated congenital heart disease.
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The human simian crease and its variants. A model for investigation of serious congenital malformation.
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Racial differentials in the prevalence rates of males with sex chromosome abnormalities (XXY, XYY) in security settings in the United States.
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Why is the XX fitter? Evidence consistent with an effect of X-heterosis in the human female from sex ratio data in offspring of first cousin marriages.
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Letter: Why is the XX fitter? Evidence consistent with an effect of X-heterosis in women from sex ratio data in offspring of first cousin marriages.
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Behavioral implications of the human XYY genotype.
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Observations on the rate of chromosome breakage in cells cultured from umbilical cord blood in relation to infant birth weight.
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Comparison of quantitative autoradiographic DNA replication patterns of human chromosomes obtained using 3H-deoxycytidine and 3H-thymidine as precursors.
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A pilot screening study of chromosome breakage in cultured blood cells from newborn infants.
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